A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986111



Internal ID19209642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:33493277..33493327hg38UCSC Ensembl
Outerchr21:34865584..34865634hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131633
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986111
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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