A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543538



Internal ID20916784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68403616..68405544hg38UCSC Ensembl
chr2:68630748..68632676hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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