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dbVar

Database of genomic structural variation

nsv2794369

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:545

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: 132 SVs from 34 studies. See in: genome view

Submitted genomic65,375,872-65,376,416

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv2794369	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	65,375,872	65,376,416
nsv2794369	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	65,842,590	65,843,134

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv13702598	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
nssv13702598	Submitted genomic		NC_000014.9:g.6537 5872_65376416inv	GRCh38 (hg38)		NC_000014.9	Chr14	65,375,872	65,376,416
nssv13702598	Remapped	Perfect	NC_000014.8:g.6584 2590_65843134inv	GRCh37.p13	First Pass	NC_000014.8	Chr14	65,842,590	65,843,134

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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