A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892665



Internal ID169288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11413315..11418137hg38UCSC Ensembl
chr1:11473372..11478194hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384823
hg194823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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