A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905677



Internal ID4591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5666290..5676100hg38UCSC Ensembl
chr1:5726350..5736160hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg389811
hg199811
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905677
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.496923


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