A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035434



Internal ID21944777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66635260..66636501hg38UCSC Ensembl
chr15:66927598..66928839hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035434
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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