A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356923



Internal ID21014476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47505769..47509911hg38UCSC Ensembl
chr3:47547259..47551401hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384143
hg194143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101984
Samples
Known GenesELP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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