A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105344



Internal ID21291677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:220473707..220477891hg38UCSC Ensembl
Innerchr1:220647049..220651233hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg384185
hg194185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113958
Supporting Variants
Samplessample78
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105344
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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