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dbVar

Database of genomic structural variation

nsv5954187

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: 161 SVs from 32 studies. See in: genome view

Submitted genomic136,885,361-136,885,361

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5954187	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	136,885,361	136,885,361
nsv5954187	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	137,806,515	137,806,515

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17412387	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17412387	Submitted genomic		NC_000004.12:g.136 885361_136885362in s239	GRCh38 (hg38)		NC_000004.12	Chr4	136,885,361	136,885,361
nssv17412387	Remapped	Perfect	NC_000004.11:g.137 806515_137806516in s239	GRCh37.p13	First Pass	NC_000004.11	Chr4	137,806,515	137,806,515

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.

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