A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1743229



Internal ID12906347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89273960..89274020hg38UCSC Ensembl
chr13:89926214..89926274hg19UCSC Ensembl
chr13:88724215..88724275hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2e22
Supporting Variantsessv4163717
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1743229
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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