A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947903



Internal ID18594750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45103267..45161734hg38UCSC Ensembl
Innerchr10:45598715..45657182hg19UCSC Ensembl
Innerchr10:44918721..44977188hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3858468
hg1958468
hg1858468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1842676, nssv1842673, nssv1842675, nssv1842667, nssv1842670, nssv1842671, nssv1842672, nssv1842674, nssv1842668, nssv1842669
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD30BP3, RSU1P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947903
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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