A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331508



Internal ID22233906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11514163..11514241hg38UCSC Ensembl
chr10:11556162..11556240hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527235
Supporting Variants
SamplesHG00733
Known GenesUSP6NL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331508
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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