A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069043



Internal ID18980069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46644217..46646218hg38UCSC Ensembl
chr10:46903399..46905400hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772395
SamplesKWP1
Known GenesFAM35BP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069043
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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