A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1449360



Internal ID12265796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156328046..156328046hg38UCSC Ensembl
chr1:156297837..156297837hg19UCSC Ensembl
chr1:154564461..154564461hg18UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38142
hg19142
hg18142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3823298
SamplesHuRef
Known GenesCCT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1449360
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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