A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550520



Internal ID20923661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109587845..109588336hg38UCSC Ensembl
chr2:110345422..110345913hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4077n223
Supporting Variantsnssv18256472
Samples
Known GenesSEPT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550520
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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