A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815801



Internal ID15763071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77521165..77539089hg38UCSC Ensembl
Innerchr13:78095300..78113224hg19UCSC Ensembl
Innerchr13:76993301..77011225hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3817925
hg1917925
hg1817925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562375
Supporting Variants
Samples
Known GenesSCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv815801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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