A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243864



Internal ID20810904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68992677..68994049hg38UCSC Ensembl
chr17:66988818..66990190hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585422
Supporting Variants
Samples
Known GenesABCA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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