A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4306677



Internal ID11589215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105382356..105382665hg38UCSC Ensembl
chr13:106034706..106035015hg19UCSC Ensembl
chr13:104832707..104833016hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38310
hg19310
hg18310
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1282846
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4306677
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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