A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133516



Internal ID19258310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63830447..63832047hg38UCSC Ensembl
Outerchr20:62461800..62463400hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2295n106
Supporting Variantsnssv3969078
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133516
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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