A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589144



Internal ID20962215
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 StatusM
Merged Variants
Supporting Variantsnssv18242471
Samples
Known GenesITGB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589144
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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