A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614702



Internal ID16402111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76535987..76545077hg38UCSC Ensembl
Innerchr9:79150903..79159993hg19UCSC Ensembl
Innerchr9:78340723..78349813hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389091
hg199091
hg189091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12765n54
Supporting Variantsnssv1137586
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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