A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562609



Internal ID16350018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85420565..85732317hg38UCSC Ensembl
Innerchr13:85994700..86306452hg19UCSC Ensembl
Innerchr13:84892701..85204453hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38311753
hg19311753
hg18311753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148664
SamplesHGDP00586
Known GenesLINC00351
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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