A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8932n54



Internal ID22776827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5733576..5780257hg38UCSC Ensembl
chr4:5735303..5781984hg19UCSC Ensembl
chr4:5786204..5832885hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3846682
hg1946682
hg1846682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593490, nsv593491
SamplesNINDS_36
Known GenesEVC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8932n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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