A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4777n100



Internal ID22790864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75357235..75636809hg38UCSC Ensembl
chr3:75406386..75685960hg19UCSC Ensembl
chr3:75489076..75768650hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38279575
hg19279575
hg18279575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012818, nsv1003188, nsv1007938, nsv1013514, nsv1013196, nsv1012206, nsv1005725, nsv1012911, nsv997991, nsv1003210, nsv1002163, nsv1001704, nsv1007816, nsv1002249, nsv1012365, nsv1005563, nsv999532, nsv1005617, nsv997814, nsv998064, nsv998533, nsv999390, nsv1009813, nsv999685, nsv999722, nsv1013221, nsv1006121, nsv1012783, nsv1009638, nsv1009577, nsv1001625, nsv1006308, nsv1010138, nsv1001019
Samples
Known GenesFAM86DP, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4777n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss753
Observed Complex0
Frequencyn/a


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