A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960025



Internal ID18869476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8756767..8790867hg38UCSC Ensembl
Outerchr21:9645600..9679700hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3834101
hg1934101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110374
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960025
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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