A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181628



Internal ID20748668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101908109..101909077hg38UCSC Ensembl
chr10:103667866..103668834hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445426
Supporting Variants
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00108


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