A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740754



Internal ID18715000
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 StatusS
Merged Variantsesv3542007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740754
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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