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dbVar

Database of genomic structural variation

nsv6622673

Organism: Homo sapiens

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

Variant Calls:3
Validation:Not tested
Clinical Assertions: No
Region Size:32,707

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: 178 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):60,436,854-60,469,560

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6622673	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	60,436,854	60,469,560
nsv6622673	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	60,903,572	60,936,278

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18283203	duplication	OSC2302	SNP array	Probe signal intensity	15
nssv18284253	duplication	OSC2590	SNP array	Probe signal intensity	16
nssv18292035	duplication	OSC3996	SNP array	Probe signal intensity	9

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18283203	Remapped	Perfect	NC_000014.9:g.(?_6 0436854)_(60469560 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	60,436,854	60,469,560
nssv18284253	Remapped	Perfect	NC_000014.9:g.(?_6 0436854)_(60469560 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	60,436,854	60,469,560
nssv18292035	Remapped	Perfect	NC_000014.9:g.(?_6 0436854)_(60469560 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	60,436,854	60,469,560
nssv18283203	Submitted genomic		NC_000014.8:g.(?_6 0903572)_(60936278 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	60,903,572	60,936,278
nssv18284253	Submitted genomic		NC_000014.8:g.(?_6 0903572)_(60936278 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	60,903,572	60,936,278
nssv18292035	Submitted genomic		NC_000014.8:g.(?_6 0903572)_(60936278 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	60,903,572	60,936,278

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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