A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12460n54



Internal ID19004636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:707077..708225hg38UCSC Ensembl
chr9:707077..708225hg19UCSC Ensembl
chr9:697077..698225hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381149
hg191149
hg181149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613041, nsv613043, nsv613042
Samples
Known GenesKANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12460n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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