A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3785e59



Internal ID22765005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44027928..44032626hg38UCSC Ensembl
chr7:44067527..44072225hg19UCSC Ensembl
chr7:44034052..44038750hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg384699
hg194699
hg184699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3409486, esv3335929
SamplesNA19239, NA19240
Known GenesRASA4CP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3785e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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