A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689772



Internal ID15054960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45026562..45031860hg38UCSC Ensembl
Innerchr15:45027562..45030860hg38UCSC Ensembl
Outerchr15:45025562..45032860hg38UCSC Ensembl
chr15:45318760..45324058hg19UCSC Ensembl
Innerchr15:45319760..45323058hg19UCSC Ensembl
Outerchr15:45317760..45325058hg19UCSC Ensembl
chr15:43106052..43111350hg18UCSC Ensembl
Innerchr15:43107052..43110350hg18UCSC Ensembl
Outerchr15:43105052..43112350hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385299
hg195299
hg185299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3401551
Supporting Variants
SamplesNA19239
Known GenesSORD
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689772
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer