A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv35e59



Internal ID22761255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7567505..7570103hg38UCSC Ensembl
chr1:7627565..7630163hg19UCSC Ensembl
chr1:7550152..7552750hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3413631, esv3418027, esv3352384
SamplesNA19238, NA19239, NA19240
Known GenesCAMTA1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv35e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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