A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569505



Internal ID20942576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11122341..11124855hg38UCSC Ensembl
chr5:11122453..11124967hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382515
hg192515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267167
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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