A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523556



Internal ID21847915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3694023..3694189hg38UCSC Ensembl
chr1:3610587..3610753hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984201
Supporting Variants
Samples
Known GenesTP73
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523556
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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