A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949149



Internal ID33451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61104506..61136348hg38UCSC Ensembl
chr4:61970224..62002066hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3831843
hg1931843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949149
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.166927


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