A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375282



Internal ID21032835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114721541..114722012hg38UCSC Ensembl
chr3:114440388..114440859hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092781
Samples
Known GenesZBTB20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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