A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613830



Internal ID16401239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23979688..24035013hg38UCSC Ensembl
Innerchr9:23979686..24035011hg19UCSC Ensembl
Innerchr9:23969686..24025011hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3855326
hg1955326
hg1855326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131827
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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