A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071741



Internal ID18975916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10427537..10427599hg38UCSC Ensembl
chr21:11084858..11084920hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771564
SamplesKWP1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071741
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