A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614502



Internal ID16401911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62435331..62453800hg38UCSC Ensembl
Innerchr9:46746632..46765101hg19UCSC Ensembl
Innerchr9:46586628..46605097hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3818470
hg1918470
hg1818470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134681
Samples
Known GenesKGFLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614502
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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