A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971969



Internal ID18607185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96759..113009hg38UCSC Ensembl
Innerchr11:96759..113009hg19UCSC Ensembl
Innerchr11:86759..103009hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3816251
hg1916251
hg1816251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1871884, nssv1871888, nssv1871889, nssv1871892, nssv1871890, nssv1871893, nssv1871891, nssv1871886, nssv1871885, nssv1871887
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)nsv971969
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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