A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284190



Internal ID20493408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146971363..146971479hg38UCSC Ensembl
chr4:147892515..147892631hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284190
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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