A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549489



Internal ID21873844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82619876..82619938hg38UCSC Ensembl
chr4:83541029..83541091hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998420
Supporting Variants
Samples
Known GenesLINC00575
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549489
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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