A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5396n54



Internal ID22773291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:948888..952193hg38UCSC Ensembl
chr17:852128..855433hg19UCSC Ensembl
chr17:798878..802183hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383306
hg193306
hg183306
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574110, nsv574134
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5396n54
Frequency
Sample Size17421
Observed Gain57
Observed Loss5
Observed Complex0
Frequencyn/a


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