A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356624



Internal ID21014177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24051113..24097467hg38UCSC Ensembl
chr3:24092604..24138958hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3846355
hg1946355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356624
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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