A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892695



Internal ID19183515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54786525..54849067hg38UCSC Ensembl
Outerchr15:54786525..54849067hg38UCSC Ensembl
Innerchr15:55078723..55141265hg19UCSC Ensembl
Outerchr15:55078723..55141265hg19UCSC Ensembl
Innerchr15:52866015..52928557hg18UCSC Ensembl
Outerchr15:52866015..52928557hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3862543
hg1962543
hg1862543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789228
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892695
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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