A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904180



Internal ID3604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62827505..62827525hg38UCSC Ensembl
chr1:63293176..63293196hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542566
Supporting Variants
Samples
Known GenesATG4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904180
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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