A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971999



Internal ID18607215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33189060..33190527hg38UCSC Ensembl
Innerchr11:33210606..33212073hg19UCSC Ensembl
Innerchr11:33167182..33168649hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381468
hg191468
hg181468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881320, nssv1881324, nssv1881328, nssv1881325, nssv1881329, nssv1881323, nssv1881321, nssv1881322, nssv1881326, nssv1881327
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCSTF3-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971999
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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