A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577585



Internal ID21526039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108933081..108933226hg38UCSC Ensembl
chr1:109475703..109475848hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060284
SamplesNA19238
Known GenesCLCC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577585
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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