A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv691n100



Internal ID22786778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24083828..24107259hg38UCSC Ensembl
chr10:24372757..24396188hg19UCSC Ensembl
chr10:24412763..24436194hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3823432
hg1923432
hg1823432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041437, nsv1047756, nsv1044891, nsv1050320
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)dgv691n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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