A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615312



Internal ID16056035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126572421..126644710hg38UCSC Ensembl
Innerchr9:129334700..129406989hg19UCSC Ensembl
Innerchr9:128374521..128446810hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3872290
hg1972290
hg1872290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12868n54
Supporting Variantsnssv1141350
Samples
Known GenesLMX1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615312
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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