A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073212



Internal ID19317500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25663808..25664809hg38UCSC Ensembl
chr3:25705299..25706300hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766234
SamplesKWP1
Known GenesTOP2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073212
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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