A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890854



Internal ID168076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153417880..153459217hg38UCSC Ensembl
chr1:153390356..153431693hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3841338
hg1941338
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563935
Supporting Variants
Samples
Known GenesS100A7, S100A7A, S100A7L2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890854
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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