A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4776n100



Internal ID22790863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75357235..75546018hg38UCSC Ensembl
chr3:75406386..75595169hg19UCSC Ensembl
chr3:75489076..75677859hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38188784
hg19188784
hg18188784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001097, nsv1009229, nsv1002268, nsv1001845, nsv1005929, nsv999260, nsv1006717, nsv1013432, nsv997646, nsv1005064, nsv1010264, nsv1004088, nsv1013786, nsv1011256, nsv998752, nsv1004017
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)dgv4776n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss202
Observed Complex0
Frequencyn/a


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