A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242891



Internal ID20809931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38842413..38842603hg38UCSC Ensembl
chr17:36998666..36998856hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242891
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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