A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949664



Internal ID22725110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141269102..141269102hg38UCSC Ensembl
chr6:141590239..141590239hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949664
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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