A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981536



Internal ID21890879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155469053..155474596hg38UCSC Ensembl
chr1:155438844..155444387hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg385544
hg195544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530667
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981536
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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