A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242598



Internal ID20809638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62885984..62886405hg38UCSC Ensembl
chr17:60963345..60963766hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583515
Supporting Variants
Samples
Known GenesMIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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