A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541076



Internal ID20914362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22564540..22565200hg38UCSC Ensembl
chr2:22787412..22788072hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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