A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541427



Internal ID20914708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47925110..47925314hg38UCSC Ensembl
chr2:48152249..48152453hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541427
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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