A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243725



Internal ID20810765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59156772..59157420hg38UCSC Ensembl
chr17:57234133..57234781hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587625
Supporting Variants
Samples
Known GenesPRR11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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