A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330276



Internal ID22197178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10400329..10402511hg38UCSC Ensembl
chr10:10442292..10444474hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382183
hg192183
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217894
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330276
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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