A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4773n100



Internal ID22790860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75347667..75845369hg38UCSC Ensembl
chr3:75396818..75894520hg19UCSC Ensembl
chr3:75479508..75977210hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38497703
hg19497703
hg18497703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014162, nsv998082, nsv999731, nsv1005724, nsv999953
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4773n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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