A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360793



Internal ID21018346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64064436..64070339hg38UCSC Ensembl
chr3:64050112..64056015hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385904
hg195904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101474
Samples
Known GenesPRICKLE2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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