A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224170



Internal ID20791210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124366501..124381400hg38UCSC Ensembl
chr8:125378742..125393641hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3814900
hg1914900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419843
Supporting Variants
Samples
Known GenesTMEM65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224170
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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