A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975902



Internal ID18264423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35374236..35375599hg38UCSC Ensembl
Innerchr11:35395783..35397146hg19UCSC Ensembl
Innerchr11:35352359..35353722hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381364
hg191364
hg181364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881476, nssv1881474, nssv1881475, nssv1881481, nssv1881473, nssv1881478, nssv1881479, nssv1881480, nssv1881477, nssv1881472
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesSLC1A2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975902
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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