A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540852



Internal ID20914140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74469288..74469994hg38UCSC Ensembl
chr2:74696415..74697121hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3929n223
Supporting Variantsnssv18258366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540852
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