A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316623



Internal ID22233525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88327672..88328616hg38UCSC Ensembl
chr4:89248824..89249768hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199519
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316623
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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