A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243249



Internal ID20810289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78772595..78773432hg38UCSC Ensembl
chr17:76768677..76769514hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578232
Supporting Variants
Samples
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243249
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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