A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6665



Internal ID15190513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28595445..28608350hg38UCSC Ensembl
Outerchr16:28606766..28619671hg19UCSC Ensembl
Outerchr16:28514267..28527172hg18UCSC Ensembl
Outerchr16:28514267..28527172hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812098
hg1912098
hg1812098
hg1712098
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1775
Supporting Variants
SamplesNA12156
Known GenesSULT1A1, SULT1A2
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)nssv6665
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer