A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446621



Internal ID21104174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124916201..124917600hg38UCSC Ensembl
chr10:126604770..126606169hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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