A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2554n100



Internal ID19012922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34379873..34585552hg38UCSC Ensembl
chr15:34672074..34877753hg19UCSC Ensembl
chr15:32459366..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38205680
hg19205680
hg18205680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043386, nsv1051982, nsv1050002, nsv1045290, nsv1047561, nsv1053907, nsv1045360, nsv1050109
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2554n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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