A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9107



Internal ID15534757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:33387702..33432559hg38UCSC Ensembl
Outerchr13:33961839..34006696hg19UCSC Ensembl
Outerchr13:32859839..32904696hg18UCSC Ensembl
Outerchr13:32859839..32904696hg17UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3844858
hg1944858
hg1844858
hg1744858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv993
Supporting Variants
SamplesNA12156
Known GenesSTARD13
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)nssv9107
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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