A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181391



Internal ID20748431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128077799..128111236hg38UCSC Ensembl
chr10:129876063..129909500hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3833438
hg1933438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446946
Supporting Variants
Samples
Known GenesMKI67, PTPRE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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