A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051133



Internal ID20618173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108953847..108959011hg38UCSC Ensembl
chr1:109496469..109501633hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385165
hg195165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333876
Supporting Variants
Samples
Known GenesCLCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01483


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