A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094419



Internal ID22003652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42281067..42281067hg38UCSC Ensembl
chr12:42674869..42674869hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094419
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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