A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253551



Internal ID20820591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1489798..1490822hg38UCSC Ensembl
chr20:1470443..1471468hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381025
hg191026
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597890
Supporting Variants
Samples
Known GenesSIRPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253551
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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