A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528977



Internal ID21853334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176905638..176905700hg38UCSC Ensembl
chr1:176874774..176874836hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982186
Supporting Variants
Samples
Known GenesASTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528977
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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