A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381216



Internal ID21038769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145176601..145179500hg38UCSC Ensembl
chr4:146097753..146100652hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212010
Samples
Known GenesOTUD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381216
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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