A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557795



Internal ID18412185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44045069..44045678hg38UCSC Ensembl
Outerchr21:44045054..44045720hg38UCSC Ensembl
Innerchr21:45464950..45465559hg19UCSC Ensembl
Outerchr21:45464935..45465601hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9756542
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557795
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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