A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947907



Internal ID18594754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45186984..45199552hg38UCSC Ensembl
Innerchr10:45682432..45695000hg19UCSC Ensembl
Innerchr10:45002438..45015006hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812569
hg1912569
hg1812569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1843947, nssv1843952, nssv1843951, nssv1843949, nssv1843946, nssv1843945, nssv1843954, nssv1843950, nssv1843953, nssv1843948
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)nsv947907
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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