A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10103



Internal ID15542694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75998299..76030741hg38UCSC Ensembl
Outerchr16:76032197..76064639hg19UCSC Ensembl
Outerchr16:74589698..74622140hg18UCSC Ensembl
Outerchr16:74589698..74622140hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg387056
hg197056
hg187056
hg177056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1882
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10103
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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