A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947740



Internal ID18247901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13104039..13105540hg38UCSC Ensembl
Innerchr10:13146039..13147540hg19UCSC Ensembl
Innerchr10:13186045..13187546hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381502
hg191502
hg181502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832303, nssv1832306, nssv1832304, nssv1832299, nssv1832308, nssv1832302, nssv1832301, nssv1832307, nssv1832300, nssv1832305
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesOPTN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947740
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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