A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373799



Internal ID21031352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168651896..168666730hg38UCSC Ensembl
chr3:168369684..168384518hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3814835
hg1914835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097377
Samples
Known GenesEGFEM1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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