A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088758



Internal ID21280976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58512288..58514285hg38UCSC Ensembl
Innerchr10:60272048..60274045hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381998
hg191998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115910
Supporting Variants
Samplessample304
Known GenesBICC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088758
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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