A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548033



Internal ID20921232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:117210785..117490468hg38UCSC Ensembl
chr2:117968361..118248044hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38279684
hg19279684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548033
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