A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953650



Internal ID16955837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44970586..45002585hg38UCSC Ensembl
Outerchr21:46390501..46422500hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3832000
hg1932000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000701
SamplesBILGI_BIOE
Known GenesFAM207A, LINC00162, LINC00163
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953650
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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