A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069684



Internal ID21978917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196960739..196960739hg38UCSC Ensembl
chr3:196687610..196687610hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547593
Samples
Known GenesPIGZ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069684
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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