A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361785



Internal ID21019338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9726181..9731277hg38UCSC Ensembl
chr3:9767865..9772961hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg385097
hg195097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104869
Samples
Known GenesCPNE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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