A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844366



Internal ID15791636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68426648..68467128hg38UCSC Ensembl
Innerchr15:68718987..68759467hg19UCSC Ensembl
Innerchr15:66506041..66546521hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3840481
hg1940481
hg1840481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569806
Supporting Variants
Samples
Known GenesITGA11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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