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

dbVar

Database of genomic structural variation

nsv6112617

Organism: Homo sapiens

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

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

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: 565 SVs from 38 studies. See in: genome view

Submitted genomic79,912,137-79,912,137

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112617	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	79,912,137	79,912,137
nsv6112617	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	77,672,137	77,672,137

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17635026	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17635026	Submitted genomic		NC_000018.10:g.799 12137_79912138ins6 1	GRCh38 (hg38)		NC_000018.10	Chr18	79,912,137	79,912,137
nssv17635026	Remapped	Perfect	NC_000018.9:g.7767 2137_77672138ins61	GRCh37.p13	First Pass	NC_000018.9	Chr18	77,672,137	77,672,137

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