A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101456



Internal ID21283557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11761581..11787893hg38UCSC Ensembl
Innerchr19:11872396..11898708hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3826313
hg1926313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117741
Supporting Variants
Samplessample346
Known GenesZNF441
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101456
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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