A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790736



Internal ID21236074
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 StatusM
Merged Variants
Supporting Variantsnssv13681678, nssv13693556
Samples
Known GenesPAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790736
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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