A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982200



Internal ID18617395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20532143..20534478hg38UCSC Ensembl
Innerchr9:20532141..20534476hg19UCSC Ensembl
Innerchr9:20522141..20524476hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382336
hg192336
hg182336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524148, nssv2524144, nssv2524151, nssv2524150, nssv2524147, nssv2524146, nssv2524153, nssv2524145, nssv2524149, nssv2524152
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMLLT3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982200
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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