A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14811362



Internal ID4145533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78910002..78920881hg38UCSC Ensembl
chr13:79484137..79495016hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3810880
hg1910880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632807
Supporting Variants
SamplesHG03753
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14811362
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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