A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972001



Internal ID18607217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39765900..39768236hg38UCSC Ensembl
Innerchr11:39787450..39789786hg19UCSC Ensembl
Innerchr11:39744026..39746362hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382337
hg192337
hg182337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1882197, nssv1882202, nssv1882201, nssv1882200, nssv1882194, nssv1882195, nssv1882196, nssv1882203, nssv1882198, nssv1882199
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)nsv972001
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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