A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586834



Internal ID20959905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39451701..39452033hg38UCSC Ensembl
chr17:37607954..37608286hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586834
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