A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110379



Internal ID19275114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9922172..10009872hg38UCSC Ensembl
Outerchr21:10400200..10487900hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3887701
hg1987701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2306n106
Supporting Variantsnssv3960030
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110379
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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