A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176163



Internal ID15508235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136619086..136723384hg38UCSC Ensembl
Innerchr9:139513538..139617836hg19UCSC Ensembl
Innerchr9:138633359..138737657hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38104299
hg19104299
hg18104299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615978
Supporting Variants
Samples1780862388_A
Known GenesAGPAT2, EGFL7, FAM69B, MIR126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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