A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2667n100



Internal ID22788754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99814277..100060270hg38UCSC Ensembl
chr15:100354482..100600475hg19UCSC Ensembl
chr15:98172005..98417998hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38245994
hg19245994
hg18245994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051364, nsv1053108, nsv1047996, nsv1040747, nsv1038027, nsv1045147, nsv1052757, nsv1053635, nsv1049220
Samples
Known GenesADAMTS17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2667n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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