A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593257



Internal ID20966328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40846302..40847562hg38UCSC Ensembl
chr17:39002554..39003814hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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