A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1775



Internal ID15199652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28595445..28619570hg38UCSC Ensembl
Outerchr16:28606766..28630891hg19UCSC Ensembl
Outerchr16:28514267..28538392hg18UCSC Ensembl
Outerchr16:28514267..28538392hg17UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv9314, nssv6665, nssv9528
SamplesNA18517, NA18507, NA12156
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)nsv1775
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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