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

dbVar

Database of genomic structural variation

nsv5958460

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 124 SVs from 23 studies. See in: genome view

Submitted genomic179,710,707-179,710,707

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958460	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	179,710,707	179,710,707
nsv5958460	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	179,137,708	179,137,708

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17425631	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17425631	Submitted genomic		NC_000005.10:g.179 710707_179710708in s226	GRCh38 (hg38)		NC_000005.10	Chr5	179,710,707	179,710,707
nssv17425631	Remapped	Perfect	NC_000005.9:g.1791 37708_179137709ins 226	GRCh37.p13	First Pass	NC_000005.9	Chr5	179,137,708	179,137,708

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