A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983027



Internal ID18271535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59477533..59479704hg38UCSC Ensembl
Innerchr11:59245006..59247177hg19UCSC Ensembl
Innerchr11:59001582..59003753hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382172
hg192172
hg182172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1892411, nssv1892419, nssv1892410, nssv1892418, nssv1892415, nssv1892417, nssv1892412, nssv1892413, nssv1892416, nssv1892414
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR4D10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983027
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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