A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104885



Internal ID21289861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:192238338..192250184hg38UCSC Ensembl
Innerchr1:192207468..192219314hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3811847
hg1911847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117544
Supporting Variants
Samplessample52
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104885
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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