A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266250



Internal ID20833290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12490219..12693664hg38UCSC Ensembl
chr5:12490331..12693776hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38203446
hg19203446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557227
Supporting Variants
Samples
Known GenesCT49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266250
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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