A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2638n100



Internal ID19013006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84115810..84584129hg38UCSC Ensembl
chr15:84784562..85127360hg19UCSC Ensembl
chr15:82575566..82928364hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38468320
hg19342799
hg18352799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041110, nsv1045457, nsv1053185, nsv1049185, nsv1043106, nsv1045946, nsv1035817, nsv1042705, nsv1050691, nsv1054646, nsv1052911, nsv1054792
Samples
Known GenesDNM1P41, EFTUD1P1, GOLGA6L4, GOLGA6L5P, LINC00933, 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)dgv2638n100
Frequency
Sample Size29084
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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