A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13807118



Internal ID4172206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52444619..52480445hg38UCSC Ensembl
chr10:54204379..54240205hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3835827
hg1935827
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623248
Supporting Variants
SamplesHG03772
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13807118
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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