A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144186



Internal ID343390
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 StatusM
Merged Variants
Supporting Variantsnssv17040136
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144186
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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