A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906725



Internal ID5266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95735201..95735252hg38UCSC Ensembl
chr1:96200757..96200808hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540777
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906725
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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