A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597076



Internal ID6984390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96617545..96628051hg38UCSC Ensembl
chr3:96336389..96346895hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810507
hg1910507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv913e214
Supporting Variantsessv11074008, essv11074012, essv11074014, essv11074007, essv11074009, essv11074010, essv11074011, essv11074013
SamplesHG03378, HG02122, HG03372, NA19319, NA19315, HG02943, NA18873, NA19900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597076
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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