A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542537



Internal ID18396927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141920666..141926703hg38UCSC Ensembl
Outerchr7:141920517..141926776hg38UCSC Ensembl
Innerchr7:141620466..141626503hg19UCSC Ensembl
Outerchr7:141620317..141626576hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386260
hg196260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741284
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542537
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