A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578241



Internal ID20951312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58198241..58198384hg38UCSC Ensembl
chr17:56275602..56275745hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245980
Samples
Known GenesEPX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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