A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369458



Internal ID21027011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57177301..57187000hg38UCSC Ensembl
chr3:57211329..57221028hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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