A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691852



Internal ID21213708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74117050..74117131hg38UCSC Ensembl
chr11:73828095..73828176hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790468
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691852
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.5


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