A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5399n54



Internal ID22773294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:948940..949808hg38UCSC Ensembl
chr17:852180..853048hg19UCSC Ensembl
chr17:798930..799798hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38869
hg19869
hg18869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574114, nsv574122
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5399n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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