A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14307454



Internal ID22273624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69106861..69107454hg38UCSC Ensembl
chr3:69156012..69156605hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203395
Supporting Variants
SamplesNA19239
Known GenesLMOD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14307454
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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