A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578232



Internal ID20951303
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 StatusM
Merged Variants
Supporting Variantsnssv18243249
Samples
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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