A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084829



Internal ID21994062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62486255..62486255hg38UCSC Ensembl
chr12:62880035..62880035hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613148
Samples
Known GenesMON2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084829
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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