A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv813696



Internal ID16107652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69825214..69832892hg38UCSC Ensembl
Innerchr13:70399346..70407024hg19UCSC Ensembl
Innerchr13:69297347..69305025hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg387679
hg197679
hg187679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562212
Supporting Variants
Samples
Known GenesKLHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv813696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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