A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615374



Internal ID16056097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127770709..127866860hg38UCSC Ensembl
Innerchr9:130532988..130629139hg19UCSC Ensembl
Innerchr9:129572809..129668960hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3896152
hg1996152
hg1896152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176500
Samples1780862075_A
Known GenesAK1, CDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615374
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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