A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554287



Internal ID21878642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40894363..40894363hg38UCSC Ensembl
chr4:40896380..40896380hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067822
Supporting Variants
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554287
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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