A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761362



Internal ID18735608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58713768..58713878hg38UCSC Ensembl
chr1:59179440..59179550hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761362
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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