A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1490838



Internal ID12653960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14833959..14833959hg38UCSC Ensembl
chr4:14835583..14835583hg19UCSC Ensembl
chr4:14444681..14444681hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38132
hg19132
hg18132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3846835
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1490838
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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