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dbVar

Database of genomic structural variation

nsv5968950

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: 95 SVs from 21 studies. See in: genome view

Submitted genomic50,401,375-50,401,375

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968950	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	50,401,375	50,401,375
nsv5968950	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	50,904,632	50,904,632

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17406747	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17406747	Submitted genomic		NC_000019.10:g.504 01375_50401376ins1 12	GRCh38 (hg38)		NC_000019.10	Chr19	50,401,375	50,401,375
nssv17406747	Remapped	Perfect	NC_000019.9:g.5090 4632_50904633ins11 2	GRCh37.p13	First Pass	NC_000019.9	Chr19	50,904,632	50,904,632

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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