A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687557



Internal ID21209412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:881639..881639hg38UCSC Ensembl
chr11:881639..881639hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790750
Supporting Variants
Samples
Known GenesCHID1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687557
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.666667


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