A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948201



Internal ID18595047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117873299..117874059hg38UCSC Ensembl
Innerchr10:119632810..119633570hg19UCSC Ensembl
Innerchr10:119622800..119623560hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38761
hg19761
hg18761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866869, nssv1866865, nssv1866867, nssv1866868, nssv1866874, nssv1866872, nssv1866871, nssv1866870, nssv1866873, nssv1866866
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)nsv948201
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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