A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995999



Internal ID7080309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150135401..150135401hg38UCSC Ensembl
chr3:149853188..149853188hg19UCSC Ensembl
chr3:151335878..151335878hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570317
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995999
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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