A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615294



Internal ID16402703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125737335..125747771hg38UCSC Ensembl
Innerchr9:128499614..128510050hg19UCSC Ensembl
Innerchr9:127539435..127549871hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810437
hg1910437
hg1810437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141319
Samples
Known GenesPBX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615294
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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