A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901875



Internal ID2046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46522955..46523101hg38UCSC Ensembl
chr1:46988627..46988773hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901875
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01483


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