A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644964



Internal ID7031715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:846296..877968hg38UCSC Ensembl
chr20:826939..858611hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3831673
hg1931673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16109457
SamplesHG02085
Known GenesANGPT4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644964
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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