A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090845



Internal ID21274215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79477431..79480036hg38UCSC Ensembl
Innerchr9:82092346..82094951hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115957
Supporting Variants
Samplessample203
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090845
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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