A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541699



Internal ID20914981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62335816..62341236hg38UCSC Ensembl
chr3:62321491..62326911hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg385421
hg195421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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