A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374362



Internal ID21031915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64018401..64026300hg38UCSC Ensembl
chr3:64004077..64011976hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212952
Samples
Known GenesPSMD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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