A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690748



Internal ID21212602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68397512..68397577hg38UCSC Ensembl
chr15:68689851..68689916hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795278
Supporting Variants
Samples
Known GenesITGA11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690748
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.758065


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