A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137870



Internal ID15991056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85701971..85788297hg38UCSC Ensembl
Innerchr9:88316886..88403212hg19UCSC Ensembl
Innerchr9:87506706..87593032hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3886327
hg1986327
hg1886327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614774
Supporting Variants
Samples
Known GenesAGTPBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137870
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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