A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446191



Internal ID21103744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12393188..12415445hg38UCSC Ensembl
chr10:12435187..12457444hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822258
hg1922258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183981
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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