A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2618n100



Internal ID22788705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70674404..70714570hg38UCSC Ensembl
chr15:70966743..71006909hg19UCSC Ensembl
chr15:68753797..68793963hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3840167
hg1940167
hg1840167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040838, nsv1050722
Samples
Known GenesUACA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2618n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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