A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945660



Internal ID31109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3299340..3304222hg38UCSC Ensembl
chr4:3301067..3305949hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384883
hg194883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945660
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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