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dbVar

Database of genomic structural variation

nsv5667163

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:133,774

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: 1324 SVs from 96 studies. See in: genome view

Submitted genomic15,028,058-15,161,831

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667163	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	15,028,058	15,161,831
nsv5667163	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	15,121,915	15,255,688

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17093073	inversion	SAMN00006579	Optical mapping, Sequencing	Optical mapping, Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17093073	Submitted genomic		NC_000016.10:g.150 28058_15161831inv	GRCh38 (hg38)		NC_000016.10	Chr16	15,028,058	15,161,831
nssv17093073	Remapped	Perfect	NC_000016.9:g.1512 1915_15255688inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	15,121,915	15,255,688

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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