A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075569



Internal ID18969898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11653242..11655643hg38UCSC Ensembl
chr1:11713299..11715700hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763456
SamplesKWP1
Known GenesFBXO2, FBXO44
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075569
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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