Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4715972

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: 138 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):189,549,896-189,549,897

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4715972	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	189,549,896	189,549,897
nsv4715972	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	189,267,685	189,267,686

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16238607	inversion	M456	Sequencing	Paired-end mapping	1	4,735

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16238607	Remapped	Perfect	NC_000003.12:g.189 549896_189549897in v	GRCh38.p12	First Pass	NC_000003.12	Chr3	189,549,896	189,549,897
nssv16238607	Submitted genomic		NC_000003.11:g.189 267685_189267686in v	GRCh37 (hg19)		NC_000003.11	Chr3	189,267,685	189,267,686

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.

You are here: NCBI