A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550083



Internal ID20923235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31836749..31837569hg38UCSC Ensembl
chr2:32061818..32062638hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550083
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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