A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981897



Internal ID21891240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16166185..16166241hg38UCSC Ensembl
chr1:16492680..16492736hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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