A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896220



Internal ID171626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214600237..214605555hg38UCSC Ensembl
chr1:214773580..214778898hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385319
hg195319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444004
Supporting Variants
Samples
Known GenesCENPF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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