A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2928e59



Internal ID22764148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7639325..7640723hg38UCSC Ensembl
chr4:7641052..7642450hg19UCSC Ensembl
chr4:7691952..7693350hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3430783, esv3365716, esv3427504
SamplesNA19238, NA19239, NA19240
Known GenesSORCS2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2928e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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