A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2658n100



Internal ID20154274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90290495..90466149hg38UCSC Ensembl
chr15:90833727..91009381hg19UCSC Ensembl
chr15:88634731..88810385hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38175655
hg19175655
hg18175655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040505, nsv1046519, nsv1035920, nsv1045218, nsv1038283
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2658n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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