A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369706



Internal ID21027259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168885096..168885631hg38UCSC Ensembl
chr3:168602884..168603419hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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