A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264870



Internal ID20831910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157204907..157205867hg38UCSC Ensembl
chr4:158126059..158127019hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264870
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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