A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv966n100



Internal ID19011334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103385173..103553473hg38UCSC Ensembl
chr10:105144930..105313230hg19UCSC Ensembl
chr10:105134920..105303220hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38168301
hg19168301
hg18168301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045702, nsv1042525
Samples
Known GenesCALHM1, CALHM2, CALHM3, MIR1307, NEURL1, PDCD11, TAF5, USMG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv966n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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