A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225951



Internal ID22368925
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340311
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225951
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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