A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356292



Internal ID21013845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49905284..49920604hg38UCSC Ensembl
chr3:49942717..49958037hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3815321
hg1915321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209371
Samples
Known GenesMON1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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