A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586843



Internal ID20959914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73093602..73094060hg38UCSC Ensembl
chr13:73667740..73668198hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586843
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