A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646276



Internal ID7033021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61713674..61737698hg38UCSC Ensembl
chr20:60288730..60312754hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3824025
hg1924025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16220427, essv16220422, essv16220420, essv16220417, essv16220410, essv16220415, essv16220416, essv16220413, essv16220428, essv16220411, essv16220419, essv16220429, essv16220418, essv16220425, essv16220414, essv16220412, essv16220424, essv16220421, essv16220423, essv16220426
SamplesNA20853, NA21089, HG03603, HG04182, NA21103, HG03777, NA20869, HG04020, NA20884, NA21119, NA20875, HG03756, NA20867, NA21124, HG03858, NA21113, NA21125, NA20847, NA21102, NA21091
Known GenesCDH4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646276
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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