A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374692



Internal ID21032245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127773519..127775848hg38UCSC Ensembl
chr3:127492362..127494691hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382330
hg192330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094114
Samples
Known GenesMGLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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