A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14342884



Internal ID22142618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105380601..105380705hg38UCSC Ensembl
chr8:106392829..106392933hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225047
Supporting Variants
SamplesHG00513
Known GenesZFPM2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14342884
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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