A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14890450



Internal ID4892266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107183484..107185132hg38UCSC Ensembl
Innerchr13:107183485..107185131hg38UCSC Ensembl
Outerchr13:107183483..107185133hg38UCSC Ensembl
chr13:107835832..107837480hg19UCSC Ensembl
Innerchr13:107835833..107837479hg19UCSC Ensembl
Outerchr13:107835831..107837481hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381649
hg191649
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633483
Supporting Variants
SamplesHG03052
Known GenesFAM155A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14890450
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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