A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9528



Internal ID15193100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28603589..28619570hg38UCSC Ensembl
Outerchr16:28614910..28630891hg19UCSC Ensembl
Outerchr16:28522411..28538392hg18UCSC Ensembl
Outerchr16:28522411..28538392hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812552
hg1912552
hg1812552
hg1712552
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1775
Supporting Variants
SamplesNA18507
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)nssv9528
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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