A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451219



Internal ID21108772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35322620..35365145hg38UCSC Ensembl
chr10:35611548..35654073hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3842526
hg1942526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181453
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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