A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563695



Internal ID20936766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3473844..3474529hg38UCSC Ensembl
chr6:3474078..3474763hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563695
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