A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2517n100



Internal ID19012885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30313356..30688830hg38UCSC Ensembl
chr15:30605559..30981033hg19UCSC Ensembl
chr15:28392851..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38375475
hg19375475
hg18375475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052176, nsv1045010, nsv1036312, nsv1044912
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, LOC100288637, LOC101059918, 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)dgv2517n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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