A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645800



Internal ID7032548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39041198..39066499hg38UCSC Ensembl
chr20:37669841..37695142hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3825302
hg1925302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16182091, essv16182093, essv16182089, essv16182092, essv16182090
SamplesNA19377, NA20884, NA19921, NA19440, NA19454
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645800
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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