A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624148



Internal ID7011004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89035358..89040529hg38UCSC Ensembl
chr10:90795115..90800286hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385172
hg195172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13890558, essv13890561, essv13890559, essv13890562, essv13890560
SamplesNA12283, NA12878, NA20885, HG01933, HG00759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624148
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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