A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562382



Internal ID16349791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697595..77698481hg38UCSC Ensembl
Innerchr13:78271730..78272616hg19UCSC Ensembl
Innerchr13:77169731..77170617hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38887
hg19887
hg18887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3262n54
Supporting Variantsnssv815808
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562382
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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