A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561085



Internal ID20934156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138301966..138302815hg38UCSC Ensembl
chr5:137637655..137638504hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266813
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561085
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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