A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765635



Internal ID17481810
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975803
Supporting Variants
SamplesHGDP00998
Known GenesMXI1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765635
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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