A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10918307



Internal ID920123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9866873..9879489hg38UCSC Ensembl
chr3:9908557..9921173hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3812617
hg1912617
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595254
Supporting Variants
SamplesNA18618
Known GenesCIDEC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10918307
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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