A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv529e59



Internal ID22761749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133176958..133178456hg38UCSC Ensembl
chr10:134990462..134991960hg19UCSC Ensembl
chr10:134840452..134841950hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3391955, esv3362575
SamplesNA19239, NA19240
Known GenesKNDC1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv529e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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