A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243202



Internal ID20810242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76532709..76533589hg38UCSC Ensembl
chr17:74528791..74529671hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577958
Supporting Variants
Samples
Known GenesCYGB, PRCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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