A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085969



Internal ID21274974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:172569942..172574858hg38UCSC Ensembl
Innerchr1:172539082..172543998hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg384917
hg194917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111999
Supporting Variants
Samplessample216
Known GenesSUCO
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085969
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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