A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252544



Internal ID20819584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36247696..36248345hg38UCSC Ensembl
chr20:34835618..34836267hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599442
Supporting Variants
Samples
Known GenesAAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252544
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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