A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3945e59



Internal ID22765165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131653653..131655451hg38UCSC Ensembl
chr7:131338412..131340210hg19UCSC Ensembl
chr7:130988952..130990750hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3367320, esv3374881
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3945e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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