A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543755



Internal ID20917001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:59608096..59615120hg38UCSC Ensembl
chr2:59835231..59842255hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg387025
hg197025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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