A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623166



Internal ID6663334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49157210..49161409hg38UCSC Ensembl
chr10:50365255..50369454hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796119, essv13796118
SamplesHG02582, NA18943
Known GenesC10orf128
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623166
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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