A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766059



Internal ID18740305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15188195..15190587hg38UCSC Ensembl
Outerchr6:15187995..15190658hg38UCSC Ensembl
Innerchr6:15188426..15190818hg19UCSC Ensembl
Outerchr6:15188226..15190889hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382664
hg192664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766059
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