A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768322



Internal ID19308904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10475684..10476289hg38UCSC Ensembl
chr21:11036168..11036773hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071405
Supporting Variants
SamplesKWP1
Known GenesBAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768322
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer