A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615221



Internal ID16402630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113681989..113709956hg38UCSC Ensembl
Innerchr9:116444269..116472236hg19UCSC Ensembl
Innerchr9:115484090..115512057hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3827968
hg1927968
hg1827968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176143
Samples1780854392_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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