A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243242



Internal ID20810282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78084039..78084630hg38UCSC Ensembl
chr17:76080120..76080711hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592473
Supporting Variants
Samples
Known GenesTNRC6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243242
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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