A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645573



Internal ID6685635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24941553..25007313hg38UCSC Ensembl
chr20:24922189..24987949hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3865761
hg1965761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16166441
SamplesHG03539
Known GenesACSS1, APMAP, CST7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645573
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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