A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591402



Internal ID20964473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63596117..63596728hg38UCSC Ensembl
chr17:61673476..61674087hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591402
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