A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1801e59



Internal ID22763021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69961545..69961958hg38UCSC Ensembl
chr17:67957686..67958099hg19UCSC Ensembl
chr17:65469281..65469694hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38414
hg19414
hg18414
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302987, esv3302516
SamplesNA18502, NA18947, NA11995, NA18592, NA18508, NA11920, NA11931, NA12751, NA18504, NA18510, NA18550, NA18519, NA18489, NA18547, NA18916, NA11992, NA11918, NA18571, NA12761, NA19137, NA19238, NA12044, NA18520, NA19239, NA18973, NA18638, NA10847, NA18951, NA12489, NA12878, NA18516, NA18579, NA18871, NA18907, NA18573, NA18499, NA11894, NA18912, NA12892, NA19099, NA19257, NA18523, NA18576, NA12716, NA11881, NA19108, NA18961, NA18517, NA19240, NA07051, NA18943, NA06986, NA12749, NA19093, NA19102, NA18552, NA18505, NA19129, NA12006, NA18562
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1801e59
Frequency
Sample Size185
Observed Gain60
Observed Loss0
Observed Complex0
Frequencyn/a


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