A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9314



Internal ID15193579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28602192..28607927hg38UCSC Ensembl
Outerchr16:28613513..28619248hg19UCSC Ensembl
Outerchr16:28521014..28526749hg18UCSC Ensembl
Outerchr16:28521014..28526749hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3813437
hg1913437
hg1813437
hg1713437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1775
Supporting Variants
SamplesNA18517
Known GenesSULT1A1
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)nssv9314
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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