A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678836



Internal ID21200697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8953717..8953911hg38UCSC Ensembl
chr16:9047574..9047768hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796431
Supporting Variants
Samples
Known GenesUSP7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.714286


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