A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531648



Internal ID21856004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90927094..90927208hg38UCSC Ensembl
chr1:91392651..91392765hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984982
Supporting Variants
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531648
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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