A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241621



Internal ID20808661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28162196..28162623hg38UCSC Ensembl
chr17:26489222..26489649hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593935
Supporting Variants
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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