A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242471



Internal ID20809511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47271940..47287731hg38UCSC Ensembl
chr17:45349306..45365097hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3815792
hg1915792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589144
Supporting Variants
Samples
Known GenesITGB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242471
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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