A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366144



Internal ID21023697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16611176..16617234hg38UCSC Ensembl
chr3:16652683..16658741hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386059
hg196059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4804n223
Supporting Variantsnssv18097956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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