A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975939



Internal ID18611146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63327501..63342222hg38UCSC Ensembl
Innerchr11:63094973..63109694hg19UCSC Ensembl
Innerchr11:62851549..62866270hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3814722
hg1914722
hg1814722
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1892946, nssv1892947, nssv1892949, nssv1892942, nssv1892948, nssv1892940, nssv1892941, nssv1892944, nssv1892945, nssv1892943
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975939
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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