A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9416n54



Internal ID20142840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183098458..183099974hg38UCSC Ensembl
chr4:184019611..184021127hg19UCSC Ensembl
chr4:184256605..184258121hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381517
hg191517
hg181517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596341, nsv596339, nsv596337, nsv596336, nsv596338
Samples
Known GenesWWC2, WWC2-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9416n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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