A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593704



Internal ID20966775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10617917..10619066hg38UCSC Ensembl
chr17:10521234..10522383hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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