A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243830



Internal ID20810870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67971389..67971533hg38UCSC Ensembl
chr17:65967505..65967649hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589041
Supporting Variants
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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