A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252554



Internal ID20819594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36659612..36660084hg38UCSC Ensembl
chr20:35288015..35288487hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596398
Supporting Variants
Samples
Known GenesNDRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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