A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259256



Internal ID20826296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113807229..113808112hg38UCSC Ensembl
chr3:113526076..113526959hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563606
Supporting Variants
Samples
Known GenesATP6V1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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