A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14307456



Internal ID22204401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69110387..69110724hg38UCSC Ensembl
chr3:69159538..69159875hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525222
Supporting Variants
SamplesHG00732
Known GenesLMOD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14307456
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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