A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765376



Internal ID20541236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57520536..57520536hg38UCSC Ensembl
chr16:57554448..57554448hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295937
Samples
Known GenesCCDC102A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765376
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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