A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645567



Internal ID6685629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24879101..25011663hg38UCSC Ensembl
chr20:24859737..24992299hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38132563
hg19132563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16164052, essv16164051
SamplesHG03539, NA19454
Known GenesACSS1, APMAP, CST7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645567
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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