A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978538



Internal ID18898309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:89608208..89608287hg38UCSC Ensembl
Outerchr14:90074552..90074631hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115976
Supporting Variants
SamplesKWS2
Known GenesFOXN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978538
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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