A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076311



Internal ID21985544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41918796..41918796hg38UCSC Ensembl
chr4:41920813..41920813hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076311
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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