A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3364150



Internal ID15211128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64387394..64388787hg38UCSC Ensembl
Innerchr6:64387394..64388787hg38UCSC Ensembl
Outerchr6:64386414..64390533hg38UCSC Ensembl
chr6:65097287..65098680hg19UCSC Ensembl
Innerchr6:65097287..65098680hg19UCSC Ensembl
Outerchr6:65096307..65100426hg19UCSC Ensembl
chr6:65155246..65155401hg18UCSC Ensembl
Innerchr6:65155246..65155401hg18UCSC Ensembl
Outerchr6:65154266..65157147hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381394
hg191394
hg18156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652342
SamplesNA19240
Known GenesEYS
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3364150
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