A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196192



Internal ID20763232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100512435..100608282hg38UCSC Ensembl
chr10:102272192..102368039hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3895848
hg1995848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453002
Supporting Variants
Samples
Known GenesHIF1AN, NDUFB8, SEC31B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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