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dbVar

Database of genomic structural variation

nsv5941767

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:208

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

Submitted genomic85,584,707-85,584,914

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5941767	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	85,584,707	85,584,914
nsv5941767	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	86,051,051	86,051,258

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17373308	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17373308	Submitted genomic		NC_000014.9:g.8558 4707_85584914del	GRCh38 (hg38)		NC_000014.9	Chr14	85,584,707	85,584,914
nssv17373308	Remapped	Perfect	NC_000014.8:g.8605 1051_86051258del	GRCh37.p13	First Pass	NC_000014.8	Chr14	86,051,051	86,051,258

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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