A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1026263



Internal ID12189388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6321542..6321542hg38UCSC Ensembl
chr5:6321655..6321655hg19UCSC Ensembl
chr5:6374655..6374655hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381058
hg191058
hg181058
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4081567
SamplesHuRef
Known GenesFLJ33360
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1026263
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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