A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189135



Internal ID20756175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76808784..76869758hg38UCSC Ensembl
chr10:78568542..78629516hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3860975
hg1960975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451274
Supporting Variants
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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