A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904727



Internal ID3973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77168629..77168629hg38UCSC Ensembl
chr1:77634314..77634314hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542263
Supporting Variants
Samples
Known GenesPIGK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904727
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.187582


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