A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099101



Internal ID22008334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103768604..103768604hg38UCSC Ensembl
chr12:104162382..104162382hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099101
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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