A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615411



Internal ID16056134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128727172..128829871hg38UCSC Ensembl
Innerchr9:131489451..131592150hg19UCSC Ensembl
Innerchr9:130529272..130631971hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38102700
hg19102700
hg18102700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1143261
Samples
Known GenesC9orf114, ENDOG, LOC100506100, TBC1D13, ZER1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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