A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614576



Internal ID16055299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485202..69500582hg38UCSC Ensembl
Innerchr9:72100118..72115498hg19UCSC Ensembl
Innerchr9:71289938..71305318hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3815381
hg1915381
hg1815381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12743n54
Supporting Variantsnssv1137120
Samples
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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