A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957213



Internal ID38783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155181036..155181089hg38UCSC Ensembl
chr4:156102188..156102241hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957213
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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