A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615370



Internal ID16056093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127731234..127824409hg38UCSC Ensembl
Innerchr9:130493513..130586688hg19UCSC Ensembl
Innerchr9:129533334..129626509hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3893176
hg1993176
hg1893176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12879n54
Supporting Variantsnssv1176498
Samples1780862275_A
Known GenesCDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C, TOR2A, TTC16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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