A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944467



Internal ID21364536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109597453..109597453hg38UCSC Ensembl
chr4:110518609..110518609hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200759
SamplesHG002
Known GenesCCDC109B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944467
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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