A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4857n100



Internal ID22790944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128662394..128708009hg38UCSC Ensembl
chr3:128381237..128426852hg19UCSC Ensembl
chr3:129863927..129909542hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3845616
hg1945616
hg1845616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002202, nsv1014517, nsv1013037, nsv1011364
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)dgv4857n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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