A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452206



Internal ID21109759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124032316..124035828hg38UCSC Ensembl
chr10:125791832..125795344hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383513
hg193513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978489
Samples
Known GenesCHST15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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