A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689810



Internal ID14749170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84217996..84223194hg38UCSC Ensembl
Innerchr15:84218996..84222194hg38UCSC Ensembl
Outerchr15:84216996..84224194hg38UCSC Ensembl
chr15:84886748..84891946hg19UCSC Ensembl
Innerchr15:84887748..84890946hg19UCSC Ensembl
Outerchr15:84885748..84892946hg19UCSC Ensembl
chr15:82677752..82682950hg18UCSC Ensembl
Innerchr15:82678752..82681950hg18UCSC Ensembl
Outerchr15:82676752..82683950hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385199
hg195199
hg185199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3326972
Supporting Variants
SamplesNA19240
Known GenesLOC388152
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689810
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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