A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623199



Internal ID6663367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50405964..50409298hg38UCSC Ensembl
chr10:52165724..52169058hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg383335
hg193335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13802474, essv13802475, essv13802476, essv13802478, essv13802479, essv13802477
SamplesHG02808, NA21125, HG03631, HG00375, NA19701, NA18924
Known GenesSGMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623199
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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