A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236802



Internal ID20803842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133297240..133303938hg38UCSC Ensembl
chr8:134309483..134316181hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg386699
hg196699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418168
Supporting Variants
Samples
Known GenesNDRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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