A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690657



Internal ID21212513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982124..60982124hg38UCSC Ensembl
chr11:60749596..60749596hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790678
Supporting Variants
Samples
Known GenesCD6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690657
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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