A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529358



Internal ID21853715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157126860..157126922hg38UCSC Ensembl
chr1:157096652..157096714hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981407
Supporting Variants
Samples
Known GenesETV3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529358
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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