A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv655n100



Internal ID20152271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1133579..1495256hg38UCSC Ensembl
chr10:1179519..1537451hg19UCSC Ensembl
chr10:1169519..1527451hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38361678
hg19357933
hg18357933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045618, nsv1047911
Samples
Known GenesADARB2, LINC00200
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv655n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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