A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451911



Internal ID21109464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22220001..22263300hg38UCSC Ensembl
chr10:22508930..22552229hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3843300
hg1943300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183791
Samples
Known GenesLOC100130992
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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