A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536317



Internal ID21860672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42771365..42772413hg38UCSC Ensembl
chr2:42998505..42999553hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989216
Supporting Variants
Samples
Known GenesHAAO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536317
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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