A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266891



Internal ID20833931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140186994..140187636hg38UCSC Ensembl
chr5:139566579..139567221hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558392
Supporting Variants
Samples
Known GenesCYSTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266891
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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