A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982901



Internal ID18618096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123859605..123865918hg38UCSC Ensembl
Innerchr10:125619121..125625434hg19UCSC Ensembl
Innerchr10:125609111..125615424hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386314
hg196314
hg186314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764307
SamplesHGDP00665
Known GenesCPXM2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982901
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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