A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947824



Internal ID18247985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33056583..33059106hg38UCSC Ensembl
Innerchr10:33345511..33348034hg19UCSC Ensembl
Innerchr10:33385517..33388040hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382524
hg192524
hg182524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1839868, nssv1839874, nssv1839875, nssv1839870, nssv1839867, nssv1839872, nssv1839876, nssv1839869, nssv1839871, nssv1839873
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)nsv947824
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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