A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363853



Internal ID21021406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4895514..4897606hg38UCSC Ensembl
chr3:4937198..4939290hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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