A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275915



Internal ID20485133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38734171..38734171hg38UCSC Ensembl
chr4:38735792..38735792hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275915
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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