A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548306



Internal ID20921498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27742343..27743616hg38UCSC Ensembl
chr2:27965210..27966483hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548306
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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