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dbVar

Database of genomic structural variation

nsv4716086

Organism: Homo sapiens

Study:nstd195 (Mwapagha et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2

Publication(s):Mwapagha 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: 96 SVs from 18 studies. See in: genome view

Remapped(Score: Perfect):133,336,962-133,336,963

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4716086	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	133,336,962	133,336,963
nsv4716086	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	133,658,100	133,658,101

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16242075	inversion	M478	Sequencing	Paired-end mapping	1	4,557

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16242075	Remapped	Perfect	NC_000006.12:g.133 336962_133336963in v	GRCh38.p12	First Pass	NC_000006.12	Chr6	133,336,962	133,336,963
nssv16242075	Submitted genomic		NC_000006.11:g.133 658100_133658101in v	GRCh37 (hg19)		NC_000006.11	Chr6	133,658,100	133,658,101

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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