A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614773



Internal ID16402182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85508022..85525582hg38UCSC Ensembl
Innerchr9:88122937..88140497hg19UCSC Ensembl
Innerchr9:87312757..87330317hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3817561
hg1917561
hg1817561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137869
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614773
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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