A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739330



Internal ID18713576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548459..143551001hg38UCSC Ensembl
Outerchr6:143548210..143551332hg38UCSC Ensembl
Innerchr6:143869596..143872138hg19UCSC Ensembl
Outerchr6:143869347..143872469hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383123
hg193123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739330
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