A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4008e59



Internal ID22765228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156237197..156238295hg38UCSC Ensembl
chr7:156029891..156030989hg19UCSC Ensembl
chr7:155722652..155723750hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3431145, esv3346379
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4008e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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