A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv810366



Internal ID15757636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49468847..49512130hg38UCSC Ensembl
Innerchr13:50042983..50086266hg19UCSC Ensembl
Innerchr13:48940984..48984267hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3843284
hg1943284
hg1843284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561615
Supporting Variants
Samples
Known GenesPHF11, SETDB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv810366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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