A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975803



Internal ID18264324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110258102..110260979hg38UCSC Ensembl
Innerchr10:112017860..112020737hg19UCSC Ensembl
Innerchr10:112007850..112010727hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382878
hg192878
hg182878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765635
SamplesHGDP00998
Known GenesMXI1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975803
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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