A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442703



Internal ID21100256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21419759..21460723hg38UCSC Ensembl
chr10:21708688..21749652hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3840965
hg1940965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442703
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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