A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3740374



Internal ID11674810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46466753..46467818hg38UCSC Ensembl
chr13:47040888..47041953hg19UCSC Ensembl
chr13:45938889..45939954hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381066
hg191066
hg181066
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1527313
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3740374
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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