A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557766



Internal ID20930837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159573364..159574076hg38UCSC Ensembl
chr6:159994396..159995108hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n223
Supporting Variantsnssv18270488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557766
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