A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566902



Internal ID20939973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164533635..164534509hg38UCSC Ensembl
chr5:163960641..163961515hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268091
Samples
Known GenesLOC102546299
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566902
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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