A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359558



Internal ID21017111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57622050..57626648hg38UCSC Ensembl
chr3:57607777..57612375hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg384599
hg194599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212280
Samples
Known GenesDENND6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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