A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561026



Internal ID20934097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139386271..139387013hg38UCSC Ensembl
chr3:139105113..139105855hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259755
Samples
Known GenesCOPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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