A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593930



Internal ID20967001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59121956..59122267hg38UCSC Ensembl
chr15:59414155..59414466hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241195
Samples
Known GenesCCNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593930
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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