A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590373



Internal ID20963444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71684599..71685209hg38UCSC Ensembl
chr17:69680740..69681350hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590373
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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