A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553787



Internal ID21878142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48063873..48063873hg38UCSC Ensembl
chr4:48065890..48065890hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553787
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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