A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182156



Internal ID20749196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43915710..43935429hg38UCSC Ensembl
chr10:44411158..44430877hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819720
hg1919720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436284
Supporting Variants
Samples
Known GenesLINC00841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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