A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764526



Internal ID20540386
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 StatusM
Merged Variants
Supporting Variantsnssv16278113
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764526
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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