A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14895752



Internal ID1251719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110080127..110109124hg38UCSC Ensembl
chr13:110732474..110761471hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3828998
hg1928998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633539
Supporting Variants
SamplesHG01105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14895752
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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