A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893404



Internal ID19184224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:29160755..29184660hg38UCSC Ensembl
Outerchr21:29160755..29184660hg38UCSC Ensembl
Innerchr21:30533076..30556981hg19UCSC Ensembl
Outerchr21:30533076..30556981hg19UCSC Ensembl
Innerchr21:29454947..29478852hg18UCSC Ensembl
Outerchr21:29454947..29478852hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3823906
hg1923906
hg1823906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782709
Samples
Known GenesMAP3K7CL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893404
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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