A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933276



Internal ID22913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46053233..46427907hg38UCSC Ensembl
chr3:46094725..46469398hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38374675
hg19374674
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563336
Supporting Variants
Samples
Known GenesCCR1, CCR2, CCR3, CCR5, CCRL2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933276
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.112395


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