A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5462n54



Internal ID22773357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15124688..15157065hg38UCSC Ensembl
chr17:15028005..15060382hg19UCSC Ensembl
chr17:14968730..15001107hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3832378
hg1932378
hg1832378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574432, nsv574435, nsv574433, nsv574434
SamplesHGDP01288, HGDP01399, HGDP00812, HGDP01180
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5462n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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