A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254329



Internal ID20821369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36942201..36942734hg38UCSC Ensembl
chr20:35570604..35571137hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595624
Supporting Variants
Samples
Known GenesSAMHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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