A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540182



Internal ID20913474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28849027..28849228hg38UCSC Ensembl
chr2:29071893..29072094hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257585
Samples
Known GenesSPDYA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540182
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