A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195879



Internal ID20762919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13076815..13083805hg38UCSC Ensembl
chr10:13118815..13125805hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386991
hg196991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447477
Supporting Variants
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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