A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892699



Internal ID18836833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56279978..56613286hg38UCSC Ensembl
Outerchr15:56259549..56692817hg38UCSC Ensembl
Innerchr15:56572176..56905484hg19UCSC Ensembl
Outerchr15:56551747..56985015hg19UCSC Ensembl
Innerchr15:54359468..54692776hg18UCSC Ensembl
Outerchr15:54339039..54772307hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38433269
hg19433269
hg18433269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790938, essv25792323
Samples
Known GenesMNS1, TEX9, ZNF280D
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892699
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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