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dbVar

Database of genomic structural variation

nsv5664778

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:42,518

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: 360 SVs from 68 studies. See in: genome view

Submitted genomic152,208,990-152,251,507

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5664778	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	152,208,990	152,251,507
nsv5664778	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	152,181,466	152,223,983

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17060809	inversion	Optical mapping, Sequencing	Optical mapping, Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17060809	Submitted genomic		NC_000001.11:g.152 208990_152251507in v	GRCh38 (hg38)		NC_000001.11	Chr1	152,208,990	152,251,507
nssv17060809	Remapped	Perfect	NC_000001.10:g.152 181466_152223983in v	GRCh37.p13	First Pass	NC_000001.10	Chr1	152,181,466	152,223,983

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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