A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436478



Internal ID21094031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129679034..129707209hg38UCSC Ensembl
chr10:131477298..131505473hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3828176
hg1928176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980582
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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