A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373152



Internal ID21030705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139801771..140232097hg38UCSC Ensembl
chr3:139520613..139950939hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38430327
hg19430327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209626
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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