A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13246164



Internal ID6665694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85901132..85919751hg38UCSC Ensembl
chr8:86913361..86931980hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3818620
hg1918620
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3617900
Supporting Variants
SamplesNA20808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13246164
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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