A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132866



Internal ID18921136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105439110..105439176hg38UCSC Ensembl
Outerchr14:105905447..105905513hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987659
SamplesKWS1
Known GenesMTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132866
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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