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dbVar

Database of genomic structural variation

nsv5910929

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:140

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: 142 SVs from 34 studies. See in: genome view

Submitted genomic114,941,264-114,941,403

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5910929	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	114,941,264	114,941,403
nsv5910929	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	116,701,023	116,701,162

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17356012	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17356012	Submitted genomic		NC_000010.11:g.114 941264_114941403de l	GRCh38 (hg38)		NC_000010.11	Chr10	114,941,264	114,941,403
nssv17356012	Remapped	Perfect	NC_000010.10:g.116 701023_116701162de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	116,701,023	116,701,162

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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