A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564658



Internal ID20937729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138301889..138302506hg38UCSC Ensembl
chr5:137637578..137638195hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266812
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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