A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192446



Internal ID20759487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129626014..129626310hg38UCSC Ensembl
chr10:131424278..131424574hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452124
Supporting Variants
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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