A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102889



Internal ID21287402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61658234..61668141hg38UCSC Ensembl
Innerchr1:62123906..62133813hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg389908
hg199908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116097
Supporting Variants
Samplessample400
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102889
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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