A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563212



Internal ID16350621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112196704..112197498hg38UCSC Ensembl
Innerchr13:112851018..112851812hg19UCSC Ensembl
Innerchr13:111899019..111899813hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38795
hg19795
hg18795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820123
Samples
Known GenesLINC01070
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563212
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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