A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8177n54



Internal ID20141601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4046892..4062242hg38UCSC Ensembl
chr3:4088576..4103926hg19UCSC Ensembl
chr3:4063576..4078926hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3815351
hg1915351
hg1815351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589415, nsv589417, nsv589416
SamplesNINDS_115, HGDP01357, NINDS_223, NINDS_51
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8177n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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