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

dbVar

Database of genomic structural variation

nsv6110208

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:61,830

Publication(s):Wu 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: 409 SVs from 56 studies. See in: genome view

Submitted genomic44,419,733-44,481,562

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6110208	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	44,419,733	44,481,562
nsv6110208	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	44,888,936	44,950,765

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17613761	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17613761	Submitted genomic		NC_000014.9:g.4441 9733_44481562inv	GRCh38 (hg38)		NC_000014.9	Chr14	44,419,733	44,481,562
nssv17613761	Remapped	Perfect	NC_000014.8:g.4488 8936_44950765inv	GRCh37.p13	First Pass	NC_000014.8	Chr14	44,888,936	44,950,765

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