A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975901



Internal ID18264422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33707564..33708162hg38UCSC Ensembl
Innerchr11:33729110..33729708hg19UCSC Ensembl
Innerchr11:33685686..33686284hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38599
hg19599
hg18599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881780, nssv1881782, nssv1881778, nssv1881779, nssv1881783, nssv1881781, nssv1881784, nssv1881785, nssv1881786, nssv1881787
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCD59
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975901
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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