A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680955



Internal ID21202815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67222632..67222632hg38UCSC Ensembl
chr11:66990103..66990103hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791098
Supporting Variants
Samples
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680955
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.95


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