A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080591



Internal ID21989824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6654728..6654728hg38UCSC Ensembl
chr12:6763894..6763894hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608822
Samples
Known GenesING4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080591
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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