A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890855



Internal ID168077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153417915..153459026hg38UCSC Ensembl
chr1:153390391..153431502hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3841112
hg1941112
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556873
Supporting Variants
Samples
Known GenesS100A7, S100A7A, S100A7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890855
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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