A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183690



Internal ID20750730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119937925..119999648hg38UCSC Ensembl
chr10:121697437..121759160hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3861724
hg1961724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443217
Supporting Variants
Samples
Known GenesMIR4682, SEC23IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183690
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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