A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088985



Internal ID21287355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58512424..58514427hg38UCSC Ensembl
Innerchr10:60272184..60274187hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382004
hg192004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114782
Supporting Variants
Samplessample40
Known GenesBICC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088985
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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