A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595003



Internal ID20968074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58471951..58472219hg38UCSC Ensembl
chr17:56549312..56549580hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245990
Samples
Known GenesHSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595003
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer