A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132057



Internal ID15985243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26154829..26194168hg38UCSC Ensembl
Innerchr9:26154827..26194166hg19UCSC Ensembl
Innerchr9:26144827..26184166hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3839340
hg1939340
hg1839340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613928
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1132057
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