A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615197



Internal ID16055920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112519756..112609117hg38UCSC Ensembl
Innerchr9:115282036..115371397hg19UCSC Ensembl
Innerchr9:114321857..114411218hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3889362
hg1989362
hg1889362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176121
SamplesNINDS_93
Known GenesKIAA1958
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer