A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982229



Internal ID18617424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41881598..41948354hg38UCSC Ensembl
Innerchr9:40283030..40349935hg19UCSC Ensembl
Innerchr9:40272921..40339935hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3866757
hg1966906
hg1867015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2533345, nssv2533340, nssv2533339, nssv2533337, nssv2533336, nssv2533342, nssv2533341, nssv2533343, nssv2533338, nssv2533344
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)nsv982229
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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