A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580101



Internal ID20953172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60713957..60714699hg38UCSC Ensembl
chr17:58791318..58792060hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243107
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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