A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539107



Internal ID20912414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39639239..39661591hg38UCSC Ensembl
chr2:39866379..39888731hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3822353
hg1922353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539107
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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