A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914568



Internal ID10456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64967836..64968183hg38UCSC Ensembl
chr2:65194970..65195317hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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