A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535734



Internal ID20909088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142375230..142384788hg38UCSC Ensembl
chr2:143132799..143142357hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg389559
hg199559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535734
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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