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dbVar

Database of genomic structural variation

nsv6621232

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:5
Validation:Not tested
Clinical Assertions: No
Region Size:51,929

Publication(s):Zarrei et al. 2023

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 231 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):95,836,284-95,888,212

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6621232	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	95,836,284	95,888,212
nsv6621232	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	95,569,448	95,621,376

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18286554	duplication	OSC0030	SNP array	Probe signal intensity	9
nssv18293178	duplication	OSC4150	SNP array	Probe signal intensity	10
nssv18299018	duplication	OSC0535	SNP array	Probe signal intensity	9
nssv18320891	duplication	OSC1000	SNP array	Probe signal intensity	7
nssv18323089	duplication	OSC1453	SNP array	Probe signal intensity	6

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18286554	Remapped	Perfect	NC_000011.10:g.(?_ 95836284)_(9588821 2_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	95,836,284	95,888,212
nssv18293178	Remapped	Perfect	NC_000011.10:g.(?_ 95836284)_(9588821 2_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	95,836,284	95,888,212
nssv18299018	Remapped	Perfect	NC_000011.10:g.(?_ 95836284)_(9588821 2_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	95,836,284	95,888,212
nssv18320891	Remapped	Perfect	NC_000011.10:g.(?_ 95836284)_(9588821 2_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	95,836,284	95,888,212
nssv18323089	Remapped	Perfect	NC_000011.10:g.(?_ 95836284)_(9588821 2_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	95,836,284	95,888,212
nssv18286554	Submitted genomic		NC_000011.9:g.(?_9 5569448)_(95621376 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	95,569,448	95,621,376
nssv18293178	Submitted genomic		NC_000011.9:g.(?_9 5569448)_(95621376 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	95,569,448	95,621,376
nssv18299018	Submitted genomic		NC_000011.9:g.(?_9 5569448)_(95621376 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	95,569,448	95,621,376
nssv18320891	Submitted genomic		NC_000011.9:g.(?_9 5569448)_(95621376 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	95,569,448	95,621,376
nssv18323089	Submitted genomic		NC_000011.9:g.(?_9 5569448)_(95621376 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	95,569,448	95,621,376

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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