A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615412



Internal ID16056135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128754559..128824961hg38UCSC Ensembl
Innerchr9:131516838..131587240hg19UCSC Ensembl
Innerchr9:130556659..130627061hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3870403
hg1970403
hg1870403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176005
SamplesHGDP00451
Known GenesC9orf114, ENDOG, TBC1D13, ZER1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615412
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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