A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819945



Internal ID16113901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111319232..111334034hg38UCSC Ensembl
Innerchr13:111971579..111986381hg19UCSC Ensembl
Innerchr13:110769580..110784382hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3814803
hg1914803
hg1814803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563183
Supporting Variants
Samples
Known GenesTEX29
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819945
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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