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dbVar

Database of genomic structural variation

nsv5672101

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:inversion
Method Type:Optical mapping, Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:46,130

Publication(s):Ebert et al. 2021

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: 772 SVs from 48 studies. See in: genome view

Submitted genomic26,979,174-27,025,303

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672101	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	26,979,174	27,025,303
nsv5672101	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	27,224,321	27,270,450

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17095228	inversion	HG02492	Optical mapping, Sequencing	Optical mapping, Sequence alignment	982

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17095228	Submitted genomic		NC_000015.10:g.269 79174_27025303inv	GRCh38 (hg38)		NC_000015.10	Chr15	26,979,174	27,025,303
nssv17095228	Remapped	Perfect	NC_000015.9:g.2722 4321_27270450inv	GRCh37.p13	First Pass	NC_000015.9	Chr15	27,224,321	27,270,450

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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