A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765391



Internal ID19315265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32740275..32741590hg38UCSC Ensembl
chr3:32781767..32783082hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072679
Supporting Variants
SamplesKWP1
Known GenesCNOT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765391
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer