A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796243



Internal ID21241581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79830901..79830901hg38UCSC Ensembl
chr16:79864798..79864798hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384237
hg194237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13679313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796243
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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