A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541821



Internal ID20915089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51453533..51454512hg38UCSC Ensembl
chr3:51487549..51488528hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38980
hg19980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260786
Samples
Known GenesVPRBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541821
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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