A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758573



Internal ID18386133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26282320..26282398hg38UCSC Ensembl
chr1:26608811..26608889hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559826
Supporting Variants
Samples
Known GenesUBXN11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758573
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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