A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2608n100



Internal ID22788695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58556528..58571327hg38UCSC Ensembl
chr15:58848727..58863526hg19UCSC Ensembl
chr15:56636019..56650818hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3814800
hg1914800
hg1814800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043560, nsv1050231
Samples
Known GenesLIPC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2608n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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