A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5412n54



Internal ID22773307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1052582..1053277hg38UCSC Ensembl
chr17:955822..956517hg19UCSC Ensembl
chr17:902572..903267hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38696
hg19696
hg18696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574166, nsv574172, nsv574173, nsv574170, nsv574171
Samples
Known GenesABR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5412n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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