A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947807



Internal ID18247968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29695109..29699043hg38UCSC Ensembl
Innerchr10:29984038..29987972hg19UCSC Ensembl
Innerchr10:30024044..30027978hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383935
hg193935
hg183935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1837299, nssv1837301, nssv1837294, nssv1837302, nssv1837303, nssv1837297, nssv1837295, nssv1837296, nssv1837300, nssv1837298
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesSVIL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947807
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer