A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5397n54



Internal ID22773292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:948888..952834hg38UCSC Ensembl
chr17:852128..856074hg19UCSC Ensembl
chr17:798878..802824hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383947
hg193947
hg183947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574123, nsv574111, nsv574117
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5397n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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