A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593232



Internal ID20966303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36958371..36959150hg38UCSC Ensembl
chr17:35315671..35316450hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242203
Samples
Known GenesAATF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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