A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554852



Internal ID20927942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230655368..230656367hg38UCSC Ensembl
chr2:231520083..231521082hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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