A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614774



Internal ID16402183
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 StatusM
Merged Variants
Supporting Variantsnssv1137870
Samples
Known GenesAGTPBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614774
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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