A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449541



Internal ID21107094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12574345..12583645hg38UCSC Ensembl
chr10:12616344..12625644hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg389301
hg199301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978650
Samples
Known GenesCAMK1D, MIR4480
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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