A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13914656



Internal ID3699406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103548266..103551296hg38UCSC Ensembl
chr10:105308023..105311053hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624418
Supporting Variants
SamplesHG03301
Known GenesNEURL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13914656
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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