A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946952



Internal ID31992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21978593..21989866hg38UCSC Ensembl
chr4:21980216..21991489hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3811274
hg1911274
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563070
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946952
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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