A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948114



Internal ID18594960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87109037..87126809hg38UCSC Ensembl
Innerchr10:88868794..88886566hg19UCSC Ensembl
Innerchr10:88858774..88876546hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3817773
hg1917773
hg1817773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1861923, nssv1861928, nssv1861921, nssv1861925, nssv1861930, nssv1861922, nssv1861929, nssv1861924, nssv1861926, nssv1861927
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM35A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948114
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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