A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613728



Internal ID16401137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19133734..19173785hg38UCSC Ensembl
Innerchr9:19133732..19173783hg19UCSC Ensembl
Innerchr9:19123732..19163783hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3840052
hg1940052
hg1840052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156446
SamplesHGDP00319
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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