A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245246



Internal ID20812286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52409512..53222775hg38UCSC Ensembl
chr17:50486872..51300136hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38813264
hg19813265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587456
Supporting Variants
Samples
Known GenesC17orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245246
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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