A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975896



Internal ID18611103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28284159..28289555hg38UCSC Ensembl
Innerchr11:28305706..28311102hg19UCSC Ensembl
Innerchr11:28262282..28267678hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg385397
hg195397
hg185397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879726, nssv1879735, nssv1879728, nssv1879730, nssv1879733, nssv1879734, nssv1879729, nssv1879731, nssv1879732, nssv1879727
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMETTL15
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975896
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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