A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2215n100



Internal ID22788302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20206113..20601040hg38UCSC Ensembl
chr15:20411366..20806345hg19UCSC Ensembl
chr15:18671380..19066359hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38394928
hg19394980
hg18394980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046804, nsv1041210, nsv1048598, nsv1035897, nsv1038038, nsv1037018, nsv1045794, nsv1046377
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2215n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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