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dbVar

Database of genomic structural variation

nsv6516967

Organism: Homo sapiens

Study:nstd223 (Sedlazeck 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:73,237

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: 474 SVs from 61 studies. See in: genome view

Submitted genomic55,332,147-55,405,383

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6516967	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	55,332,147	55,405,383
nsv6516967	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	55,843,515	55,916,751

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18199626	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18199626	Submitted genomic		NC_000019.10:g.553 32147_55405383dup	GRCh38 (hg38)		NC_000019.10	Chr19	55,332,147	55,405,383
nssv18199626	Remapped	Perfect	NC_000019.9:g.5584 3515_55916751dup	GRCh37.p13	First Pass	NC_000019.9	Chr19	55,843,515	55,916,751

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18199626	<0.001	1	39262

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