A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242548



Internal ID20809588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62060489..62060920hg38UCSC Ensembl
chr17:60137850..60138281hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591790
Supporting Variants
Samples
Known GenesMED13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242548
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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