A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901846



Internal ID2027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46240006..46242932hg38UCSC Ensembl
chr1:46705678..46708604hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382927
hg192927
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901846
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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