A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9163



Internal ID15534701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:106964717..106998396hg38UCSC Ensembl
Outerchr13:107617065..107650744hg19UCSC Ensembl
Outerchr13:106415066..106448745hg18UCSC Ensembl
Outerchr13:106415066..106448745hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385757
hg195757
hg185757
hg175757
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1174
Supporting Variants
SamplesNA12156
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)nssv9163
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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