A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568188



Internal ID20941259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138309511..138309998hg38UCSC Ensembl
chr5:137645200..137645687hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266814
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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