A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951481



Internal ID35010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82914732..82914792hg38UCSC Ensembl
chr4:83835885..83835945hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469327
Supporting Variants
Samples
Known GenesTHAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951481
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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