A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562387



Internal ID16349796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697718..77705097hg38UCSC Ensembl
Innerchr13:78271853..78279232hg19UCSC Ensembl
Innerchr13:77169854..77177233hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg387380
hg197380
hg187380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815813
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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