A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372030



Internal ID21029583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94294383..94301036hg38UCSC Ensembl
chr3:94013227..94019880hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg386654
hg196654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372030
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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