A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624645



Internal ID7011496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115866081..115908172hg38UCSC Ensembl
chr10:117625592..117667683hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3842092
hg1942092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13943568, essv13943566, essv13943565, essv13943567
SamplesHG01177, HG00736, HG01072, HG01200
Known GenesATRNL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624645
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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