A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885762



Internal ID22660748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186348461..186348510hg38UCSC Ensembl
chr1:186317593..186317642hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355059
Samples
Known GenesMIR548F1, TPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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