A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947766



Internal ID18594613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22224974..22226349hg38UCSC Ensembl
Innerchr10:22513903..22515278hg19UCSC Ensembl
Innerchr10:22553909..22555284hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381376
hg191376
hg181376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832785, nssv1832789, nssv1832792, nssv1832788, nssv1832791, nssv1832787, nssv1832790, nssv1832784, nssv1832786, nssv1832783
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)nsv947766
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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