A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975906



Internal ID18611113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38600175..38610949hg38UCSC Ensembl
Innerchr11:38621725..38632499hg19UCSC Ensembl
Innerchr11:38578301..38589075hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3810775
hg1910775
hg1810775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880741, nssv1880747, nssv1880746, nssv1880739, nssv1880742, nssv1880748, nssv1880745, nssv1880743, nssv1880744, nssv1880740
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975906
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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