A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562545



Internal ID20935616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185977553..185981060hg38UCSC Ensembl
chr3:185695342..185698849hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383508
hg193508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261249
Samples
Known GenesLOC344887
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562545
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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