A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1414



Internal ID15199291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:95863631..95897213hg38UCSC Ensembl
Outerchr14:96329968..96363550hg19UCSC Ensembl
Outerchr14:95399721..95433303hg18UCSC Ensembl
Outerchr14:95399721..95433303hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385853
hg195853
hg185853
hg175853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9235
SamplesNA12156
Known GenesLINC00617
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)nsv1414
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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