A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278113



Internal ID20487331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56584241..56584241hg38UCSC Ensembl
chr3:56618269..56618269hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764526
Supporting Variants
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278113
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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