A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9162



Internal ID15534702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:106768337..106797940hg38UCSC Ensembl
Outerchr13:107420685..107450288hg19UCSC Ensembl
Outerchr13:106218686..106248289hg18UCSC Ensembl
Outerchr13:106218686..106248289hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg386512
hg196512
hg186512
hg176512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1173
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)nssv9162
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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