A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947733



Internal ID18594580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7154164..7156812hg38UCSC Ensembl
Innerchr10:7196126..7198774hg19UCSC Ensembl
Innerchr10:7236132..7238780hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382649
hg192649
hg182649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832915, nssv1832918, nssv1832917, nssv1832920, nssv1832916, nssv1832912, nssv1832913, nssv1832919, nssv1832914, nssv1832921
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947733
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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