A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066027



Internal ID21975260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196929189..196929189hg38UCSC Ensembl
chr3:196656060..196656060hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554789
Samples
Known GenesSENP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066027
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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