A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10204n54



Internal ID19002380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178921553..178924511hg38UCSC Ensembl
chr5:178348554..178351512hg19UCSC Ensembl
chr5:178281160..178284118hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382959
hg192959
hg182959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600470, nsv600480
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10204n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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