A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614218



Internal ID16401627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38067407..38069878hg38UCSC Ensembl
Innerchr9:38067404..38069875hg19UCSC Ensembl
Innerchr9:38057404..38059875hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg382472
hg192472
hg182472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1133973
Samples
Known GenesSHB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614218
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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