A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv665n100



Internal ID22786752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5607797..5683245hg38UCSC Ensembl
chr10:5649760..5725208hg19UCSC Ensembl
chr10:5689766..5765214hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3875449
hg1975449
hg1875449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050965, nsv1038690, nsv1052519, nsv1054909, nsv1044330, nsv1039650, nsv1043251, nsv1040422, nsv1049620, nsv1041684, nsv1037709
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv665n100
Frequency
Sample Size11257
Observed Gain39
Observed Loss0
Observed Complex0
Frequencyn/a


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