A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645520



Internal ID7032269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23186564..23205868hg38UCSC Ensembl
chr20:23167201..23186505hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3819305
hg1919305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163055, essv16163065, essv16163048, essv16163050, essv16163068, essv16163062, essv16163046, essv16163064, essv16163054, essv16163056, essv16163045, essv16163049, essv16163044, essv16163059, essv16163067, essv16163071, essv16163070, essv16163047, essv16163053, essv16163043, essv16163060, essv16163051, essv16163057, essv16163066, essv16163063, essv16163072, essv16163061, essv16163073, essv16163058, essv16163074, essv16163052, essv16163069, essv16163042, essv16163041, essv16163075
SamplesNA19909, NA19092, HG03577, HG02536, NA19314, HG03572, NA19171, HG03168, HG02549, NA20287, HG02505, NA19159, NA19239, NA19025, HG03169, HG03120, NA19210, NA19707, HG02090, NA18871, HG02497, HG03085, HG02429, HG01619, NA19257, HG02799, HG02759, HG03419, HG02771, HG03565, NA18876, NA19116, HG03538, NA19312, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645520
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer