A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261506



Internal ID20828546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57064082..57064543hg38UCSC Ensembl
chr3:57098110..57098571hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552642
Supporting Variants
Samples
Known GenesARHGEF3, SPATA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261506
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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