A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614917



Internal ID16055640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94581338..94606867hg38UCSC Ensembl
Innerchr9:97343620..97369149hg19UCSC Ensembl
Innerchr9:96383441..96408970hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3825530
hg1925530
hg1825530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175999
SamplesHGDP00897
Known GenesFBP1, FBP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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