A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv656n100



Internal ID20152272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1149274..1245720hg38UCSC Ensembl
chr10:1195214..1287772hg19UCSC Ensembl
chr10:1185214..1277772hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3896447
hg1992559
hg1892559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039304, nsv1041995
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)dgv656n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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