A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582443



Internal ID20955514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68729582..68731124hg38UCSC Ensembl
chr17:66725723..66727265hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381543
hg191543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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