A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615028



Internal ID16402437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102315118..102349016hg38UCSC Ensembl
Innerchr9:105077400..105111298hg19UCSC Ensembl
Innerchr9:104117221..104151119hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3833899
hg1933899
hg1833899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140608
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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