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dbVar

Database of genomic structural variation

nsv5965841

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:88

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: 236 SVs from 27 studies. See in: genome view

Submitted genomic31,985,085-31,985,172

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965841	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	31,985,085	31,985,172
nsv5965841	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	33,357,398	33,357,485

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404815	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404815	Submitted genomic		NC_000021.9:g.3198 5085_31985172del	GRCh38 (hg38)		NC_000021.9	Chr21	31,985,085	31,985,172
nssv17404815	Remapped	Perfect	NC_000021.8:g.3335 7398_33357485del	GRCh37.p13	First Pass	NC_000021.8	Chr21	33,357,398	33,357,485

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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