A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264279



Internal ID20831319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16096967..16097131hg38UCSC Ensembl
chr4:16098590..16098754hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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