A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815814



Internal ID16109770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697928..77698532hg38UCSC Ensembl
Innerchr13:78272063..78272667hg19UCSC Ensembl
Innerchr13:77170064..77170668hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38605
hg19605
hg18605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562388
Supporting Variants
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv815814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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