A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369632



Internal ID21027185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39953932..39994419hg38UCSC Ensembl
chr3:39995423..40035910hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3840488
hg1940488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100915
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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