A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645513



Internal ID7032262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23022364..23026241hg38UCSC Ensembl
chr20:23003001..23006878hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg383878
hg193878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16160677, essv16160668, essv16160673, essv16160678, essv16160674, essv16160676, essv16160669, essv16160664, essv16160665, essv16160661, essv16160675, essv16160670, essv16160666, essv16160672, essv16160667, essv16160671, essv16160663, essv16160662
SamplesNA19222, NA20321, NA19092, NA19107, NA18519, HG02952, HG02816, HG02885, HG01284, HG03583, HG03132, NA18910, HG02497, NA18907, NA18879, NA19435, NA19380, NA19376
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645513
Frequency
Sample Size2504
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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