A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975887



Internal ID18264408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14277966..14279466hg38UCSC Ensembl
Innerchr11:14299512..14301012hg19UCSC Ensembl
Innerchr11:14256088..14257588hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381501
hg191501
hg181501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877750, nssv1877752, nssv1877745, nssv1877746, nssv1877749, nssv1877754, nssv1877753, nssv1877748, nssv1877751, nssv1877747
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesRRAS2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975887
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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