A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540910



Internal ID20914197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207414026..207414525hg38UCSC Ensembl
chr2:208278750..208279249hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540910
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