A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356776



Internal ID21014329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43764701..43767700hg38UCSC Ensembl
chr3:43806193..43809192hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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