A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983007



Internal ID18618201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44538586..44540786hg38UCSC Ensembl
Innerchr11:44560136..44562336hg19UCSC Ensembl
Innerchr11:44516712..44518912hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382201
hg192201
hg182201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1882987, nssv1882994, nssv1882990, nssv1882989, nssv1882985, nssv1882986, nssv1882991, nssv1882992, nssv1882988, nssv1882993
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)nsv983007
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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