A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13689284



Internal ID5024400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7052656..7101977hg38UCSC Ensembl
chr10:7094618..7143939hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3849322
hg1949322
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622266
Supporting Variants
SamplesNA18517
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13689284
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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