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dbVar

Database of genomic structural variation

nsv5956620

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:112

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: 121 SVs from 30 studies. See in: genome view

Submitted genomic30,623,952-30,624,063

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5956620	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	30,623,952	30,624,063
nsv5956620	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	31,019,939	31,020,050

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17391455	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17391455	Submitted genomic		NC_000022.11:g.306 23952_30624063del	GRCh38 (hg38)		NC_000022.11	Chr22	30,623,952	30,624,063
nssv17391455	Remapped	Perfect	NC_000022.10:g.310 19939_31020050del	GRCh37.p13	First Pass	NC_000022.10	Chr22	31,019,939	31,020,050

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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