A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893356



Internal ID19184176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61719332..61740822hg38UCSC Ensembl
Outerchr20:61718613..61740822hg38UCSC Ensembl
Innerchr20:60294388..60315878hg19UCSC Ensembl
Outerchr20:60293669..60315878hg19UCSC Ensembl
Innerchr20:59727783..59749273hg18UCSC Ensembl
Outerchr20:59727064..59749273hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3822210
hg1922210
hg1822210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783278, essv25787663, essv25783904, essv25785516, essv25780317, essv25779942, essv25787378
Samples
Known GenesCDH4
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893356
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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