A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539558



Internal ID20912854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170900988..170901430hg38UCSC Ensembl
chr2:171757498..171757940hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4187n223
Supporting Variantsnssv18255450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539558
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