A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1647e59



Internal ID22762867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81765079..81765646hg38UCSC Ensembl
chr16:81798684..81799251hg19UCSC Ensembl
chr16:80356185..80356752hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38568
hg19568
hg18568
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302818, esv3302609
SamplesNA12717, NA11995, NA11829, NA18561, NA11920, NA12045, NA12751, NA18959, NA18526, NA18510, NA12750, NA12155, NA18940, NA12891, NA18558, NA18960, NA18942, NA11918, NA07347, NA19138, NA12044, NA12828, NA12003, NA18579, NA18871, NA18572, NA18948, NA18566, NA12892, NA18555, NA18593, NA18576, NA18542, NA12716, NA18961, NA07051, NA18943, NA06986, NA12749, NA19093, NA19116, NA18505, NA18965, NA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1647e59
Frequency
Sample Size185
Observed Gain44
Observed Loss0
Observed Complex0
Frequencyn/a


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