A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076416



Internal ID21985649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113934405..113934405hg38UCSC Ensembl
chr4:114855561..114855561hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541030
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076416
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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