A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196776



Internal ID20763816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128104617..128106067hg38UCSC Ensembl
chr10:129902881..129904331hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381451
hg191451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454405
Supporting Variants
Samples
Known GenesMKI67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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