A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083091



Internal ID21992324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101858904..101858904hg38UCSC Ensembl
chr12:102252682..102252682hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083091
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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