A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455512



Internal ID21113065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12724075..13074244hg38UCSC Ensembl
chr10:12766074..13116244hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38350170
hg19350171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182230
Samples
Known GenesCAMK1D, CCDC3, LOC283070
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455512
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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