A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583151



Internal ID20956222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61076819..61106761hg38UCSC Ensembl
chr13:61650953..61680895hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3829943
hg1929943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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