A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615371



Internal ID16056094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127735841..127787855hg38UCSC Ensembl
Innerchr9:130498120..130550134hg19UCSC Ensembl
Innerchr9:129537941..129589955hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3852015
hg1952015
hg1852015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176499
SamplesHGDP00774
Known GenesCDK9, MIR2861, MIR3960, SH2D3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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