A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975195



Internal ID18610403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64324276..64326947hg38UCSC Ensembl
Innerchr11:64091748..64094419hg19UCSC Ensembl
Innerchr11:63848324..63850995hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382672
hg192672
hg182672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1894206, nssv1894207, nssv1894200, nssv1894205, nssv1894202, nssv1894203, nssv1894198, nssv1894199, nssv1894204, nssv1894201
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)nsv975195
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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