A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540657



Internal ID18395047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068945..152071039hg38UCSC Ensembl
Outerchr6:152068585..152071243hg38UCSC Ensembl
Innerchr6:152390080..152392174hg19UCSC Ensembl
Outerchr6:152389720..152392378hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382659
hg192659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739404
Samples
Known GenesESR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540657
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