A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4782n100



Internal ID22790869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75400451..75511978hg38UCSC Ensembl
chr3:75449602..75561129hg19UCSC Ensembl
chr3:75532292..75643819hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38111528
hg19111528
hg18111528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014324, nsv1011810, nsv1011867, nsv997344, nsv997457, nsv1011170, nsv1000468, nsv1012545, nsv1000401
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4782n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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