A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957538



Internal ID39002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139276882..139276942hg38UCSC Ensembl
chr4:140198036..140198096hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471096
Supporting Variants
Samples
Known GenesMGARP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957538
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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