A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613439



Internal ID16400848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11649257..11935261hg38UCSC Ensembl
Innerchr9:11649257..11935261hg19UCSC Ensembl
Innerchr9:11639257..11925261hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38286005
hg19286005
hg18286005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12528n54
Supporting Variantsnssv1128562
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613439
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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