A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063997



Internal ID21973230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113612604..113612604hg38UCSC Ensembl
chr4:114533760..114533760hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548214
Samples
Known GenesCAMK2D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063997
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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