A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542007



Internal ID18743083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83317181..83317460hg38UCSC Ensembl
Outerchr7:83317099..83317498hg38UCSC Ensembl
Innerchr7:82946497..82946776hg19UCSC Ensembl
Outerchr7:82946415..82946814hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740754
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542007
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