A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv901e214



Internal ID22756795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74913126..74922101hg38UCSC Ensembl
chr3:74962277..74971252hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg388976
hg198976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596587, esv3596585
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv901e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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