A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10206n54



Internal ID22778101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178921553..178926155hg38UCSC Ensembl
chr5:178348554..178353156hg19UCSC Ensembl
chr5:178281160..178285762hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384603
hg194603
hg184603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600473, nsv600477, nsv600474, nsv600479
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10206n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss65
Observed Complex0
Frequencyn/a


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