A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175997



Internal ID15877296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71551509..71622849hg38UCSC Ensembl
Innerchr13:72125641..72196981hg19UCSC Ensembl
Innerchr13:71023642..71094982hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3871341
hg1971341
hg1871341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562270
Supporting Variants
SamplesHGDP00963
Known GenesDACH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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