A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756392



Internal ID18383952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32571358..32575190hg38UCSC Ensembl
Outerchr21:32571191..32575627hg38UCSC Ensembl
Innerchr21:33943668..33947500hg19UCSC Ensembl
Outerchr21:33943501..33947937hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384437
hg194437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557645
Supporting Variants
Samples
Known GenesTCP10L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756392
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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