A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014178



Internal ID21923521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38349317..38350331hg38UCSC Ensembl
chr10:38638245..38639259hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014178
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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