A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369747



Internal ID21027300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69796479..69796771hg38UCSC Ensembl
chr3:69845630..69845922hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104408
Samples
Known GenesMITF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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