A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902000



Internal ID2131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34967611..34967857hg38UCSC Ensembl
chr1:35433212..35433458hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428984
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902000
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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