A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11223011



Internal ID4134710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169903370..169916904hg38UCSC Ensembl
chr3:169621158..169634692hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3813535
hg1913535
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598614
Supporting Variants
SamplesHG03745
Known GenesSAMD7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11223011
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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