A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5402n54



Internal ID22773297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:949100..949861hg38UCSC Ensembl
chr17:852340..853101hg19UCSC Ensembl
chr17:799090..799851hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38762
hg19762
hg18762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574136, nsv574137, nsv574133
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5402n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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