A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544594



Internal ID21868949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177302010..177302075hg38UCSC Ensembl
chr3:177019798..177019863hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992010
Supporting Variants
Samples
Known GenesLINC00501
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544594
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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