A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079413



Internal ID21988646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72966792..72966792hg38UCSC Ensembl
chr3:73015943..73015943hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555778
Samples
Known GenesGXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079413
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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