A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738463



Internal ID18713130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50798264..50798501hg38UCSC Ensembl
Outerchr6:50798230..50798572hg38UCSC Ensembl
Innerchr6:50765977..50766214hg19UCSC Ensembl
Outerchr6:50765943..50766285hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3539716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738463
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