A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3773e59



Internal ID22764993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39259728..39261426hg38UCSC Ensembl
chr7:39299327..39301025hg19UCSC Ensembl
chr7:39265852..39267550hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336748, esv3395780
SamplesNA19238, NA19239
Known GenesPOU6F2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3773e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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