A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770193



Internal ID18967404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109498019..109498420hg38UCSC Ensembl
chr9:112260299..112260700hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077172
Supporting Variants
SamplesKWP1
Known GenesPTPN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770193
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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