A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892704



Internal ID19183524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58296311..58350388hg38UCSC Ensembl
Outerchr15:58296311..58350388hg38UCSC Ensembl
Innerchr15:58588510..58642587hg19UCSC Ensembl
Outerchr15:58588510..58642587hg19UCSC Ensembl
Innerchr15:56375802..56429879hg18UCSC Ensembl
Outerchr15:56375802..56429879hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3854078
hg1954078
hg1854078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791680
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892704
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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