A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2616n100



Internal ID20154232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68312766..68350422hg38UCSC Ensembl
chr15:68605104..68642760hg19UCSC Ensembl
chr15:66392158..66429814hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3837657
hg1937657
hg1837657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044486, nsv1039597
Samples
Known GenesITGA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2616n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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