A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614575



Internal ID16055298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69545258hg38UCSC Ensembl
Innerchr9:72100051..72160174hg19UCSC Ensembl
Innerchr9:71289871..71349994hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3860124
hg1960124
hg1860124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176084
SamplesHGDP00598
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614575
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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