A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2607n100



Internal ID22788694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57340817..57494394hg38UCSC Ensembl
chr15:57633015..57786592hg19UCSC Ensembl
chr15:55420307..55573884hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38153578
hg19153578
hg18153578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040066, nsv1045486, nsv1054095, nsv1037376, nsv1051027, nsv1037339, nsv1045506, nsv1038144, nsv1050158, nsv1043074, nsv1036911, nsv1041346, nsv1038663
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2607n100
Frequency
Sample Size11257
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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