A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594742



Internal ID20967813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68369534..68370102hg38UCSC Ensembl
chr17:66365675..66366243hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243848
Samples
Known GenesARSG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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