A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4356318



Internal ID11292170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46464972..46466142hg38UCSC Ensembl
chr13:47039107..47040277hg19UCSC Ensembl
chr13:45937108..45938278hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381171
hg191171
hg181171
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1555619
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4356318
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer