A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14342856



Internal ID22307947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103466114..103467555hg38UCSC Ensembl
chr8:104478342..104479783hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228703
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14342856
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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