A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947945



Internal ID18248105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46234510..46237281hg38UCSC Ensembl
Innerchr10:47605746..47608517hg19UCSC Ensembl
Innerchr10:47075752..47078523hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382772
hg192772
hg182772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1853698, nssv1853699, nssv1853704, nssv1853702, nssv1853695, nssv1853703, nssv1853697, nssv1853700, nssv1853696, nssv1853701
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANTXRLP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947945
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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