A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314814



Internal ID22259759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109847485..109847608hg38UCSC Ensembl
chr4:110768641..110768764hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525600
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314814
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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