A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449369



Internal ID21106922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125444972..125452776hg38UCSC Ensembl
chr10:127133541..127141345hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387805
hg197805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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