A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560582



Internal ID20933653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149918674..149919497hg38UCSC Ensembl
chr5:149298237..149299060hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268688
Samples
Known GenesPDE6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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