A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039089



Internal ID93804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128106374..128108503hg38UCSC Ensembl
chr10:129904638..129906767hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382130
hg192130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507224
Supporting Variants
Samples
Known GenesMKI67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039089
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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