A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357694



Internal ID21015247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49881227..49921259hg38UCSC Ensembl
chr3:49918660..49958692hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3840033
hg1940033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209370
Samples
Known GenesMON1A, MST1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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