A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229744



Internal ID20796784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100712087..100712896hg38UCSC Ensembl
chr13:101364341..101365150hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585830
Supporting Variants
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229744
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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