A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449090



Internal ID21106643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10748159..10748448hg38UCSC Ensembl
chr10:10790122..10790411hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449090
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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