A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2639n100



Internal ID19013007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84126845..84402534hg38UCSC Ensembl
chr15:84795597..84957232hg19UCSC Ensembl
chr15:82586601..82748236hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38275690
hg19161636
hg18161636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049587, nsv1043031, nsv1047209, nsv1037502, nsv1040592, nsv1037732, nsv1041005
Samples
Known GenesDNM1P41, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2639n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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