A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2642n100



Internal ID19013010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84153209..84554155hg38UCSC Ensembl
chr15:84821961..85097386hg19UCSC Ensembl
chr15:82612965..82898390hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38400947
hg19275426
hg18285426
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036436, nsv1045761, nsv1052585
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2642n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss3
Observed Complex0
Frequencyn/a


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