A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405213



Internal ID184558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3824959..3825010hg38UCSC Ensembl
chr10:3867151..3867202hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405213
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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