A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115201



Internal ID21298467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:202738352..202741545hg38UCSC Ensembl
Innerchr1:202707480..202710673hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383194
hg193194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv106n145
Supporting Variantsnssv14096403
Samplessample361
Known GenesKDM5B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115201
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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