A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176008



Internal ID15875300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135571320..135583304hg38UCSC Ensembl
Innerchr9:138463166..138475150hg19UCSC Ensembl
Innerchr9:137602987..137614971hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3811985
hg1911985
hg1811985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615886
Supporting Variants
SamplesHGDP00666
Known GenesLOC100130954
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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