A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623866



Internal ID21815913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44645128..44645128hg38UCSC Ensembl
chr19:45148437..45148437hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110691
Supporting Variants
Samples
Known GenesPVR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623866
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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