A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4642n100



Internal ID20156258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4019632..4112924hg38UCSC Ensembl
chr3:4061316..4154608hg19UCSC Ensembl
chr3:4036316..4129608hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3893293
hg1993293
hg1893293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011680, nsv1001324, nsv1010204
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4642n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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