A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244519



Internal ID20811559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71013960..71014767hg38UCSC Ensembl
chr17:69010101..69010908hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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