A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537715



Internal ID21862070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41121856..41121856hg38UCSC Ensembl
chr4:41123873..41123873hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079878
Supporting Variants
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537715
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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