A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132908



Internal ID19281087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44971076..44971142hg38UCSC Ensembl
Outerchr21:46390991..46391057hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987702
SamplesKWS1
Known GenesFAM207A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132908
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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