A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236263



Internal ID20803303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109248995..109263381hg38UCSC Ensembl
chr8:110261224..110275610hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3814387
hg1914387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424478
Supporting Variants
Samples
Known GenesNUDCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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