A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684037



Internal ID21205892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397704..56397989hg38UCSC Ensembl
chr16:56431616..56431901hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796036
Supporting Variants
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684037
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.625


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