A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109437



Internal ID18916131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:39378598..39378669hg38UCSC Ensembl
Outerchr21:40750524..40750595hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956141
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109437
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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