A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076182



Internal ID21985415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99862267..99862267hg38UCSC Ensembl
chr3:99581111..99581111hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551956
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076182
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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