A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624607



Internal ID6664771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113679337..113732388hg38UCSC Ensembl
Innerchr10:113679487..113732238hg38UCSC Ensembl
Outerchr10:113679187..113732538hg38UCSC Ensembl
chr10:115439096..115492147hg19UCSC Ensembl
Innerchr10:115439246..115491997hg19UCSC Ensembl
Outerchr10:115438946..115492297hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3853052
hg1953052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13941253, essv13941252
SamplesNA21099, HG01757
Known GenesCASP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624607
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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