A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568775



Internal ID20941846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75561145..75572842hg38UCSC Ensembl
chr5:74856970..74868667hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3811698
hg1911698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270213
Samples
Known GenesPOLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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