A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614918



Internal ID16055641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94618315..94649755hg38UCSC Ensembl
Innerchr9:97380597..97412037hg19UCSC Ensembl
Innerchr9:96420418..96451858hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3831441
hg1931441
hg1831441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139707
Samples
Known GenesFBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614918
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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