A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv181e55



Internal ID22761131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75343222..75726932hg38UCSC Ensembl
chr3:75392373..75776083hg19UCSC Ensembl
chr3:75475063..75858773hg18UCSC Ensembl
chr3:75475063..75858773hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38383711
hg19383711
hg18383711
hg17383711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752017, esv2752018
SamplesSPC_178, BEC_540
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv181e55
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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