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dbVar

Database of genomic structural variation

nsv5966357

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:98

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: 123 SVs from 22 studies. See in: genome view

Submitted genomic36,390,760-36,390,857

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966357	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	36,390,760	36,390,857
nsv5966357	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	35,019,163	35,019,260

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17403704	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17403704	Submitted genomic		NC_000020.11:g.363 90760_36390857del	GRCh38 (hg38)		NC_000020.11	Chr20	36,390,760	36,390,857
nssv17403704	Remapped	Perfect	NC_000020.10:g.350 19163_35019260del	GRCh37.p13	First Pass	NC_000020.10	Chr20	35,019,163	35,019,260

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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