A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901668



Internal ID1910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2748000..2774000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3826001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901668
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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