A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561211



Internal ID16001934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19735717..19862366hg38UCSC Ensembl
Innerchr13:20309857..20436506hg19UCSC Ensembl
Innerchr13:19207857..19334506hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38126650
hg19126650
hg18126650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3071n54
Supporting Variantsnssv806049
Samples
Known GenesPSPC1, ZMYM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561211
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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