A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954816



Internal ID37199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107626666..107781739hg38UCSC Ensembl
chr4:108547822..108702895hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38155074
hg19155074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465622
Supporting Variants
Samples
Known GenesPAPSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954816
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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