A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976001



Internal ID18264522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130914350..130916156hg38UCSC Ensembl
Innerchr11:130784245..130786051hg19UCSC Ensembl
Innerchr11:130289455..130291261hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381807
hg191807
hg181807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1909762, nssv1909756, nssv1909765, nssv1909763, nssv1909757, nssv1909764, nssv1909758, nssv1909761, nssv1909759, nssv1909760
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesSNX19
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976001
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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