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dbVar

Database of genomic structural variation

nsv5966021

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:1,219

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: 356 SVs from 45 studies. See in: genome view

Submitted genomic36,227,295-36,228,513

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966021	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	36,227,295	36,228,513
nsv5966021	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	37,599,593	37,600,811

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17401294	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17401294	Submitted genomic		NC_000021.9:g.3622 7295_36228513del	GRCh38 (hg38)		NC_000021.9	Chr21	36,227,295	36,228,513
nssv17401294	Remapped	Perfect	NC_000021.8:g.3759 9593_37600811del	GRCh37.p13	First Pass	NC_000021.8	Chr21	37,599,593	37,600,811

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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