A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281495



Internal ID20490713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46313714..46315115hg38UCSC Ensembl
chr19:46816971..46818372hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736271
Supporting Variants
Samples
Known GenesHIF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281495
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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