A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101906



Internal ID21266794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12619373..12624463hg38UCSC Ensembl
Innerchr19:12730187..12735277hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385091
hg195091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114914
Supporting Variants
Samplessample102
Known GenesZNF791
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101906
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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