A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551981



Internal ID21876336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158187105..158187105hg38UCSC Ensembl
chr4:159108257..159108257hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551981
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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