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dbVar

Database of genomic structural variation

nsv2815681

Organism: Homo sapiens

Study:nstd137 (Huddleston et al. 2016)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:522

Publication(s):Huddleston et al. 2016

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: 225 SVs from 31 studies. See in: genome view

Submitted genomic102,423,251-102,423,772

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv2815681	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	102,423,251	102,423,772
nsv2815681	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	103,435,479	103,436,000

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv13708229	inversion	SAMN02744161	Sequencing	Local sequence assembly	47

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv13708229	Submitted genomic		NC_000008.11:g.102 423251_102423772in v	GRCh38 (hg38)		NC_000008.11	Chr8	102,423,251	102,423,772
nssv13708229	Remapped	Perfect	NC_000008.10:g.103 435479_103436000in v	GRCh37.p13	First Pass	NC_000008.10	Chr8	103,435,479	103,436,000

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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