A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364800



Internal ID21022353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65807642..65820051hg38UCSC Ensembl
chr3:65793317..65805726hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3812410
hg1912410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101600
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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