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dbVar

Database of genomic structural variation

nsv6631252

Organism: Homo sapiens

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

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:60,299

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: 315 SVs from 53 studies. See in: genome view

Remapped(Score: Perfect):67,816,618-67,876,916

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6631252	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	67,816,618	67,876,916
nsv6631252	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	68,526,511	68,586,809

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18284103	duplication	OSC2482	SNP array	Probe signal intensity	10
nssv18325519	duplication	OSC1855	SNP array	Probe signal intensity	7

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18284103	Remapped	Perfect	NC_000006.12:g.(?_ 67816618)_(6787691 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	67,816,618	67,876,916
nssv18325519	Remapped	Perfect	NC_000006.12:g.(?_ 67816618)_(6787691 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	67,816,618	67,876,916
nssv18284103	Submitted genomic		NC_000006.11:g.(?_ 68526511)_(6858680 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	68,526,511	68,586,809
nssv18325519	Submitted genomic		NC_000006.11:g.(?_ 68526511)_(6858680 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	68,526,511	68,586,809

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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