A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149942



Internal ID18851462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:39033509..39033606hg38UCSC Ensembl
Outerchr14:39502713..39502810hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998732
SamplesKWB1
Known GenesSEC23A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149942
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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