A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14340311



Internal ID22125888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38349361..38350333hg38UCSC Ensembl
chr10:38638289..38639261hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225951
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14340311
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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