A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073274



Internal ID18970092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194347570..194348471hg38UCSC Ensembl
chr3:194068299..194069200hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762076
SamplesKWP1
Known GenesCPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073274
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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