A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1555619



Internal ID12372054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46464972..46466142hg38UCSC Ensembl
chr13:47039107..47040277hg19UCSC Ensembl
chr13:45937108..45938278hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381171
hg191171
hg181171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4356318
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1555619
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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