A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815807



Internal ID16109763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697595..77698388hg38UCSC Ensembl
Innerchr13:78271730..78272523hg19UCSC Ensembl
Innerchr13:77169731..77170524hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38794
hg19794
hg18794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562381
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)nssv815807
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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