A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684441



Internal ID21206298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81704623..81704623hg38UCSC Ensembl
chr16:81738228..81738228hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796085
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684441
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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