A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887135



Internal ID22662127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108930496..108930626hg38UCSC Ensembl
chr1:109473118..109473248hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362019
Samples
Known GenesCLCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887135
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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