A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567433



Internal ID18421823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24811667..24817718hg38UCSC Ensembl
Outerchr6:24811424..24817762hg38UCSC Ensembl
Innerchr6:24811895..24817946hg19UCSC Ensembl
Outerchr6:24811652..24817990hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386339
hg196339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766180
Samples
Known GenesFAM65B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567433
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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