A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv688n100



Internal ID22786775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24047482..24092083hg38UCSC Ensembl
chr10:24336411..24381012hg19UCSC Ensembl
chr10:24376417..24421018hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3844602
hg1944602
hg1844602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036842, nsv1042938
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv688n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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