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dbVar

Database of genomic structural variation

nsv5972491

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: 125 SVs from 18 studies. See in: genome view

Submitted genomic32,445,440-32,445,440

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972491	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	32,445,440	32,445,440
nsv5972491	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	32,936,346	32,936,346

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17395570	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17395570	Submitted genomic		NC_000019.10:g.324 45440_32445441ins2 41	GRCh38 (hg38)		NC_000019.10	Chr19	32,445,440	32,445,440
nssv17395570	Remapped	Perfect	NC_000019.9:g.3293 6346_32936347ins24 1	GRCh37.p13	First Pass	NC_000019.9	Chr19	32,936,346	32,936,346

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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