A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040136



Internal ID94468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129718689..129718994hg38UCSC Ensembl
chr10:131516953..131517258hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144186
Supporting Variants
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040136
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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