A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894101



Internal ID170220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193926576..193938703hg38UCSC Ensembl
chr1:193895706..193907833hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3812128
hg1912128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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