A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229506



Internal ID20796546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35334775..35385726hg38UCSC Ensembl
chr8:35192293..35243244hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3850952
hg1950952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427648
Supporting Variants
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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