A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436534



Internal ID21094087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123984242..124004663hg38UCSC Ensembl
chr10:125743758..125764179hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3820422
hg1920422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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