A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2493n100



Internal ID22788580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28666612..28708757hg38UCSC Ensembl
chr15:28911758..28953903hg19UCSC Ensembl
chr15:26710799..26752944hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3842146
hg1942146
hg1842146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043741, nsv1051351
Samples
Known GenesGOLGA8M, HERC2P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2493n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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