A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901882



Internal ID2051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46652338..46652438hg38UCSC Ensembl
chr1:47118010..47118110hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138394
Supporting Variants
Samples
Known GenesATPAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901882
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001407


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