A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953651



Internal ID16955838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45094486..45096385hg38UCSC Ensembl
Outerchr21:46514401..46516300hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000702
SamplesBILGI_BIOE
Known GenesADARB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953651
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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