A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892640



Internal ID19183460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28243742..28290120hg38UCSC Ensembl
Outerchr15:28243742..28290120hg38UCSC Ensembl
Innerchr15:28488888..28535266hg19UCSC Ensembl
Outerchr15:28488888..28535266hg19UCSC Ensembl
Innerchr15:26162483..26208861hg18UCSC Ensembl
Outerchr15:26162483..26208861hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3846379
hg1946379
hg1846379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789104
Samples
Known GenesHERC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892640
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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