A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244605



Internal ID20811645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75207416..75207866hg38UCSC Ensembl
chr17:73203511..73203961hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592349
Supporting Variants
Samples
Known GenesNUP85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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