A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357884



Internal ID21015437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87080886..87091513hg38UCSC Ensembl
chr3:87130036..87140663hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3810628
hg1910628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104152
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer