A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645524



Internal ID6685586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23425524..23477783hg38UCSC Ensembl
chr20:23406161..23458420hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3852260
hg1952260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163731, essv16163730
SamplesHG03295, HG03304
Known GenesCST11, CSTL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645524
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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