A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114782



Internal ID21298048
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 StatusM
Merged Variantsdgv165n145
Supporting Variantsnssv14088985
Samplessample40
Known GenesBICC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114782
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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