A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616022



Internal ID16056745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137478118..137628977hg38UCSC Ensembl
Innerchr9:140372570..140523429hg19UCSC Ensembl
Innerchr9:139492391..139643250hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38150860
hg19150860
hg18150860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13012n54
Supporting Variantsnssv1148377
Samples
Known GenesARRDC1, C9orf37, DPH7, EHMT1, MRPL41, PNPLA7, ZMYND19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616022
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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