A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613396



Internal ID16400805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10657520..10686202hg38UCSC Ensembl
Innerchr9:10657520..10686202hg19UCSC Ensembl
Innerchr9:10647520..10676202hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3828683
hg1928683
hg1828683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12520n54
Supporting Variantsnssv1128516
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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