A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14898496



Internal ID3421968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110974397..111029565hg38UCSC Ensembl
chr13:111626744..111681912hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3855169
hg1955169
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633554
Supporting Variants
SamplesHG03060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14898496
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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