A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366420



Internal ID21023973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62913401..62915000hg38UCSC Ensembl
chr3:62899076..62900675hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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