A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132549



Internal ID19259081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8858367..8886467hg38UCSC Ensembl
Outerchr21:9747200..9775300hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3828101
hg1928101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987332
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132549
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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