A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982223



Internal ID18617418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39397594..39412910hg38UCSC Ensembl
Innerchr9:39397591..39412907hg19UCSC Ensembl
Innerchr9:39387591..39402907hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3815317
hg1915317
hg1815317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2532303, nssv2532306, nssv2532304, nssv2532307, nssv2532308, nssv2532309, nssv2532301, nssv2532305, nssv2532300, nssv2532302
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982223
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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