A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782709



Internal ID19175549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:29160755..29184660hg38UCSC Ensembl
Innerchr21:30533076..30556981hg19UCSC Ensembl
Innerchr21:29454947..29478852hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3823906
hg1923906
hg1823906
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893404
Supporting Variants
Samples
Known GenesMAP3K7CL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782709
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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