A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614567



Internal ID16055290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69474904..69503851hg38UCSC Ensembl
Innerchr9:72089820..72118767hg19UCSC Ensembl
Innerchr9:71279640..71308587hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3828948
hg1928948
hg1828948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137102
Samples
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614567
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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