A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796085



Internal ID21241423
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 StatusM
Merged Variants
Supporting Variantsnssv13684441
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796085
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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