A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541229



Internal ID20914513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118131346..118133012hg38UCSC Ensembl
chr2:118888922..118890588hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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