A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv966e214



Internal ID22756860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192218451..192270994hg38UCSC Ensembl
chr3:191936240..191988783hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3852544
hg1952544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3599139, esv3599141
SamplesHG00373, HG03755, HG03809, NA19010, HG03882
Known GenesFGF12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv966e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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