A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549736



Internal ID20922891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:48317241..48317808hg38UCSC Ensembl
chr2:48544380..48544947hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258086
Samples
Known GenesFOXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549736
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