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

dbVar

Database of genomic structural variation

nsv5978031

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: 252 SVs from 37 studies. See in: genome view

Submitted genomic84,326,110-84,326,110

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5978031	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	84,326,110	84,326,110
nsv5978031	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	84,359,716	84,359,716

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17369947	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17369947	Submitted genomic		NC_000016.10:g.843 26110_84326111ins5 6	GRCh38 (hg38)		NC_000016.10	Chr16	84,326,110	84,326,110
nssv17369947	Remapped	Perfect	NC_000016.9:g.8435 9716_84359717ins56	GRCh37.p13	First Pass	NC_000016.9	Chr16	84,359,716	84,359,716

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