A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595351



Internal ID6982669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13581066..13627421hg38UCSC Ensembl
chr3:13622566..13668921hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3846356
hg1946356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10931424, essv10931425
SamplesHG03490, HG03989
Known GenesFBLN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595351
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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