A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615523



Internal ID16056246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130443364..130460028hg38UCSC Ensembl
Innerchr9:133318751..133335415hg19UCSC Ensembl
Innerchr9:132308572..132325236hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3816665
hg1916665
hg1816665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176510
SamplesHGDP00663
Known GenesASS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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