A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187732



Internal ID20754772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68992104..68994983hg38UCSC Ensembl
chr10:70751860..70754739hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382880
hg192880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437971
Supporting Variants
Samples
Known GenesKIAA1279
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187732
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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