A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073217



Internal ID18969655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38113444..38113597hg38UCSC Ensembl
chr3:38154935..38155088hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764490
SamplesKWP1
Known GenesDLEC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073217
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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