A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542374



Internal ID18743450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:123996906..123997186hg38UCSC Ensembl
Outerchr7:123996800..123997255hg38UCSC Ensembl
Innerchr7:123636960..123637240hg19UCSC Ensembl
Outerchr7:123636854..123637309hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741121
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542374
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