A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948225



Internal ID18595071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127524487..127525680hg38UCSC Ensembl
Innerchr10:129322751..129323944hg19UCSC Ensembl
Innerchr10:129212741..129213934hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1869764, nssv1869759, nssv1869763, nssv1869761, nssv1869760, nssv1869765, nssv1869768, nssv1869766, nssv1869767, nssv1869762
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)nsv948225
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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