A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243354



Internal ID20810394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8789435..8800912hg38UCSC Ensembl
chr17:8692753..8704230hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3811478
hg1911478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581713
Supporting Variants
Samples
Known GenesMFSD6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00028


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