A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1394



Internal ID15545957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:91182017..91214546hg38UCSC Ensembl
Outerchr14:91648361..91680890hg19UCSC Ensembl
Outerchr14:90718114..90750643hg18UCSC Ensembl
Outerchr14:90718114..90750643hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg386887
hg196887
hg186887
hg176887
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6607
SamplesNA12156
Known GenesC14orf159
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1394
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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