A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357899



Internal ID21015452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126468940..126528611hg38UCSC Ensembl
chr3:126187783..126247454hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3859672
hg1959672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208462
Samples
Known GenesCHST13, UROC1, ZXDC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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