A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10205n54



Internal ID19002381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178921553..178925819hg38UCSC Ensembl
chr5:178348554..178352820hg19UCSC Ensembl
chr5:178281160..178285426hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384267
hg194267
hg184267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600471, nsv600484, nsv600475, nsv600482, nsv600478, nsv600476, nsv600472, nsv600481, nsv600483
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10205n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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