A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10207n54



Internal ID19002383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178923386..178926155hg38UCSC Ensembl
chr5:178350387..178353156hg19UCSC Ensembl
chr5:178282993..178285762hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382770
hg192770
hg182770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600486, nsv600485, nsv600488, nsv600487
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10207n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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