A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv34e59



Internal ID22761254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7497405..7500703hg38UCSC Ensembl
chr1:7557465..7560763hg19UCSC Ensembl
chr1:7480052..7483350hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg383299
hg193299
hg183299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3369338, esv3370220
SamplesNA19239, NA19240
Known GenesCAMTA1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv34e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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