A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1158



Internal ID15545721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:103052100..103089533hg38UCSC Ensembl
Outerchr13:103704450..103741883hg19UCSC Ensembl
Outerchr13:102502451..102539884hg18UCSC Ensembl
Outerchr13:102502451..102539884hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3837434
hg1937434
hg1837434
hg1737434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9158
SamplesNA12156
Known GenesSLC10A2
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)nsv1158
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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