A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199236



Internal ID20766276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109166504..109284128hg38UCSC Ensembl
chr1:109709126..109826750hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38117625
hg19117625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322587
Supporting Variants
Samples
Known GenesCELSR2, KIAA1324, PSRC1, SARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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