A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1914



Internal ID15199791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85866480..85901667hg38UCSC Ensembl
Outerchr16:85900086..85935273hg19UCSC Ensembl
Outerchr16:84457587..84492774hg18UCSC Ensembl
Outerchr16:84457587..84492774hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg384550
hg194550
hg184550
hg174550
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4237
SamplesNA12878
Known GenesIRF8
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)nsv1914
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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