A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2524n100



Internal ID19012892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30438488..30644082hg38UCSC Ensembl
chr15:30730691..30936285hg19UCSC Ensembl
chr15:28517983..28723577hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38205595
hg19205595
hg18205595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053382, nsv1050747, nsv1040878
Samples
Known GenesARHGAP11B, GOLGA8H, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2524n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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