A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368542



Internal ID21026095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165545401..165578800hg38UCSC Ensembl
chr3:165263189..165296588hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3833400
hg1933400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5070n223
Supporting Variantsnssv18095609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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