A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086029



Internal ID21995262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1661906..1661906hg38UCSC Ensembl
chr12:1771072..1771072hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086029
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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