A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740822



Internal ID15084014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26251610..26251610hg38UCSC Ensembl
Innerchr15:26251609..26251611hg38UCSC Ensembl
Outerchr15:26251560..26251660hg38UCSC Ensembl
chr15:26496757..26496757hg19UCSC Ensembl
Innerchr15:26496756..26496758hg19UCSC Ensembl
Outerchr15:26496707..26496807hg19UCSC Ensembl
chr15:24047850..24047850hg18UCSC Ensembl
Innerchr15:24047851..24047849hg18UCSC Ensembl
Outerchr15:24047800..24047900hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg383884
hg193884
hg183884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3402110
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740822
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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