A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1738



Internal ID15199615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:13218198..13220680hg38UCSC Ensembl
Outerchr16:13312055..13314537hg19UCSC Ensembl
Outerchr16:13219556..13222038hg18UCSC Ensembl
Outerchr16:13219556..13222038hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg386884
hg196884
hg186884
hg176884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2948
SamplesNA18555
Known GenesSHISA9
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)nsv1738
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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