A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3567843



Internal ID7039225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110907076..110907313hg38UCSC Ensembl
chr13:111559423..111559660hg19UCSC Ensembl
chr13:110357424..110357661hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38238
hg19238
hg18238
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002915
Supporting Variants
SamplesHuRef
Known GenesANKRD10
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3567843
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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