A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447046



Internal ID21104599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129584759..129593896hg38UCSC Ensembl
chr10:131383023..131392160hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg389138
hg199138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980578
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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