A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982918



Internal ID18618112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76780..96759hg38UCSC Ensembl
Innerchr11:76780..96759hg19UCSC Ensembl
Innerchr11:66780..86759hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3819980
hg1919980
hg1819980
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1871820, nssv1871823, nssv1871818, nssv1871819, nssv1871814, nssv1871816, nssv1871815, nssv1871822, nssv1871821, nssv1871817
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed deletions
lineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982918
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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