A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906704



Internal ID5251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94663165..94689547hg38UCSC Ensembl
chr1:95128721..95155103hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3826383
hg1926383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426262
Supporting Variants
Samples
Known GenesLINC01057
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906704
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007964


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