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dbVar

Database of genomic structural variation

nsv6628183

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:79,332

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: 363 SVs from 58 studies. See in: genome view

Remapped(Score: Perfect):99,225,481-99,304,812

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6628183	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	99,225,481	99,304,812
nsv6628183	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	99,841,944	99,921,275

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18311419	duplication	OSC7529	SNP array	Probe signal intensity	8
nssv18316188	duplication	OSC8263	SNP array	Probe signal intensity	8

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18311419	Remapped	Perfect	NC_000002.12:g.(?_ 99225481)_(9930481 2_?)dup	GRCh38.p12	First Pass	NC_000002.12	Chr2	99,225,481	99,304,812
nssv18316188	Remapped	Perfect	NC_000002.12:g.(?_ 99225481)_(9930481 2_?)dup	GRCh38.p12	First Pass	NC_000002.12	Chr2	99,225,481	99,304,812
nssv18311419	Submitted genomic		NC_000002.11:g.(?_ 99841944)_(9992127 5_?)dup	GRCh37 (hg19)		NC_000002.11	Chr2	99,841,944	99,921,275
nssv18316188	Submitted genomic		NC_000002.11:g.(?_ 99841944)_(9992127 5_?)dup	GRCh37 (hg19)		NC_000002.11	Chr2	99,841,944	99,921,275

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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