A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv33e59



Internal ID22761253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7103105..7104603hg38UCSC Ensembl
chr1:7163165..7164663hg19UCSC Ensembl
chr1:7085752..7087250hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3448182, esv3449661, esv3439401
SamplesNA19238, NA19239, NA19240
Known GenesCAMTA1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv33e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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