A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756204



Internal ID18730450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:13957690..13957760hg38UCSC Ensembl
chr21:15330011..15330081hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557457
Supporting Variants
Samples
Known GenesANKRD20A11P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756204
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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