A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1033e214



Internal ID22756927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149897563..149912359hg38UCSC Ensembl
chr4:150818715..150833511hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3814797
hg1914797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3602643, esv3602644
SamplesNA12889
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1033e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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