A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891830



Internal ID168748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168543248..168578925hg38UCSC Ensembl
chr1:168512486..168548163hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3835678
hg1935678
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557222
Supporting Variants
Samples
Known GenesXCL1, XCL2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891830
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.212769


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