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

dbVar

Database of genomic structural variation

nsv5978286

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: 104 SVs from 30 studies. See in: genome view

Submitted genomic18,724,789-18,724,789

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5978286	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	18,724,789	18,724,789
nsv5978286	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	18,835,599	18,835,599

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17391846	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17391846	Submitted genomic		NC_000019.10:g.187 24789_18724790ins4 55	GRCh38 (hg38)		NC_000019.10	Chr19	18,724,789	18,724,789
nssv17391846	Remapped	Perfect	NC_000019.9:g.1883 5599_18835600ins45 5	GRCh37.p13	First Pass	NC_000019.9	Chr19	18,835,599	18,835,599

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