A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1666847



Internal ID12829965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110907081..110907319hg38UCSC Ensembl
chr13:111559428..111559666hg19UCSC Ensembl
chr13:110357429..110357667hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38239
hg19239
hg18239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4158510
SamplesHuRef
Known GenesANKRD10
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1666847
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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