A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562377



Internal ID16349786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697539..77698083hg38UCSC Ensembl
Innerchr13:78271674..78272218hg19UCSC Ensembl
Innerchr13:77169675..77170219hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38545
hg19545
hg18545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815803
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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