A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242488



Internal ID20809528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47632496..47633724hg38UCSC Ensembl
chr17:45709862..45711090hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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