A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241725



Internal ID20808765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29779600..29780638hg38UCSC Ensembl
chr17:28106618..28107656hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584755
Supporting Variants
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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