A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13941368



Internal ID547158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114868720..114899216hg38UCSC Ensembl
chr10:116628479..116658975hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3830497
hg1930497
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624622
Supporting Variants
SamplesHG00238
Known GenesFAM160B1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13941368
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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