A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908816



Internal ID6665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108953847..108959026hg38UCSC Ensembl
chr1:109496469..109501648hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385180
hg195180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424969
Supporting Variants
Samples
Known GenesCLCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908816
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.021081


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