A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950845



Internal ID17299719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:20601602..20614201hg38UCSC Ensembl
Outerchr9:20601601..20614200hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3812600
hg1912600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999376
SamplesBILGI_BIOE
Known GenesMLLT3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950845
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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