A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561210



Internal ID16001933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19728834..19865880hg38UCSC Ensembl
Innerchr13:20302974..20440020hg19UCSC Ensembl
Innerchr13:19200974..19338020hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38137047
hg19137047
hg18137047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3071n54
Supporting Variantsnssv806048
Samples
Known GenesPSPC1, ZMYM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561210
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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