A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv989e214



Internal ID22756883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16368891..16405221hg38UCSC Ensembl
chr4:16370514..16406844hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3836331
hg1936331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3599754, esv3599755
SamplesHG00737, HG00610, NA19917, HG02508, NA19428, HG01431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv989e214
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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