A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271464



Internal ID20838504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50423518..50424371hg38UCSC Ensembl
chr6:50391231..50392084hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271464
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00066


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