A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792323



Internal ID18818841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56279978..56692817hg38UCSC Ensembl
Innerchr15:56572176..56985015hg19UCSC Ensembl
Innerchr15:54359468..54772307hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38412840
hg19412840
hg18412840
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892699
Supporting Variants
Samples
Known GenesMNS1, TEX9, ZNF280D
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=65
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792323
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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