A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615845



Internal ID16403254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135243814..135259654hg38UCSC Ensembl
Innerchr9:138135660..138151500hg19UCSC Ensembl
Innerchr9:137275481..137291321hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3815841
hg1915841
hg1815841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1146788
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615845
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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