A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447826



Internal ID21105379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133296612..133297399hg38UCSC Ensembl
chr10:135110116..135110903hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978605
Samples
Known GenesTUBGCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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