A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553261



Internal ID20926370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166358264..166359944hg38UCSC Ensembl
chr2:167214774..167216454hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381681
hg191681
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255842
Samples
Known GenesSCN9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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