A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984463



Internal ID21893806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60022254..60022785hg38UCSC Ensembl
chr1:60487926..60488457hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535760
Samples
Known GenesC1orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984463
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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