A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982484



Internal ID18617679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63036956..63057897hg38UCSC Ensembl
Innerchr9:66941928..66962869hg19UCSC Ensembl
Innerchr9:66681748..66702689hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820942
hg1920942
hg1820942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736775, nssv2736771, nssv2736776, nssv2736778, nssv2736770, nssv2736773, nssv2736779, nssv2736772, nssv2736777, nssv2736774
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982484
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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