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dbVar

Database of genomic structural variation

nsv3167916

Organism: Homo sapiens

Study:nstd158 (Cleal et al. 2019)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:28,154

Publication(s):Cleal et al. 2019

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: 568 SVs from 82 studies. See in: genome view

Remapped(Score: Perfect):69,231,602-69,260,565

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3167916	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	69,232,007 (-405, +405)	69,260,160 (-405, +405)
nsv3167916	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	70,097,725 (-405, +405)	70,125,878 (-405, +405)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14239845	inversion	DB68	Sequencing	Paired-end mapping	23

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14239845	Remapped	Perfect	NC_000004.12:g.(69 231602_69232412)_( 69259755_69260565) inv	GRCh38.p12	First Pass	NC_000004.12	Chr4	69,232,007 (-405, +405)	69,260,160 (-405, +405)
nssv14239845	Submitted genomic		NC_000004.11:g.(70 097320_70098130)_( 70125473_70126283) inv	GRCh37 (hg19)		NC_000004.11	Chr4	70,097,725 (-405, +405)	70,125,878 (-405, +405)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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