A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689782



Internal ID15055039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70279459..70280857hg38UCSC Ensembl
Innerchr15:70279857..70280459hg38UCSC Ensembl
Outerchr15:70278459..70281857hg38UCSC Ensembl
chr15:70571798..70573196hg19UCSC Ensembl
Innerchr15:70572196..70572798hg19UCSC Ensembl
Outerchr15:70570798..70574196hg19UCSC Ensembl
chr15:68358852..68360250hg18UCSC Ensembl
Innerchr15:68359852..68359250hg18UCSC Ensembl
Outerchr15:68357852..68361250hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3362032
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689782
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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