A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332880



Internal ID22183861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14568328..14568717hg38UCSC Ensembl
chr10:14610327..14610716hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215086
Supporting Variants
SamplesHG00731
Known GenesFAM107B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332880
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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