A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555960



Internal ID20929031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157586774..157587526hg38UCSC Ensembl
chr5:157013782..157014534hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6002n223
Supporting Variantsnssv18269421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555960
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