A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547266



Internal ID20920468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211965645..212501180hg38UCSC Ensembl
chr2:212830370..213365904hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38535536
hg19535535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258634
Samples
Known GenesERBB4, MIR548F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547266
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