A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069855



Internal ID19319411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41573844..41577892hg38UCSC Ensembl
chr15:41866042..41870090hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384049
hg194049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766402
SamplesKWP1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069855
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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