A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv899e199



Internal ID22758672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183360489..183366417hg38UCSC Ensembl
chr3:183078277..183084205hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg385929
hg195929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668001, esv2667469
SamplesNA18602
Known GenesMCF2L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv899e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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