A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16166655



Internal ID1408676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25731016..25742904hg38UCSC Ensembl
chr20:25711652..25723540hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3811889
hg1911889
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645596
Supporting Variants
SamplesHG01277
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16166655
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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