A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681678



Internal ID21203536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77332352..77332352hg38UCSC Ensembl
chr11:77043397..77043397hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790736
Supporting Variants
Samples
Known GenesPAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681678
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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