A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3776e59



Internal ID22764996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40915743..40916002hg38UCSC Ensembl
chr7:40955342..40955601hg19UCSC Ensembl
chr7:40921867..40922126hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38260
hg19260
hg18260
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302832, esv3302467
SamplesNA18502, NA12717, NA18545, NA18504, NA19190, NA18870, NA12750, NA07346, NA18563, NA18940, NA19138, NA12761, NA19238, NA19172, NA10847, NA18951, NA18605, NA12003, NA18516, NA18907, NA18537, NA11894, NA18912, NA19257, NA18909, NA07051, NA18501, NA18511, NA07000, NA18522
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3776e59
Frequency
Sample Size185
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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