A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615206



Internal ID16055929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113053118..113104996hg38UCSC Ensembl
Innerchr9:115815398..115867276hg19UCSC Ensembl
Innerchr9:114855219..114907097hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851879
hg1951879
hg1851879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12853n54
Supporting Variantsnssv1141247, nssv1176127
SamplesHGDP00199
Known GenesFAM225B, ZFP37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615206
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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