A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115620



Internal ID19269966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45797386..45799186hg38UCSC Ensembl
Outerchr21:47217300..47219100hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2413n106
Supporting Variantsnssv3977429
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115620
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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