A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9160



Internal ID15534704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:104319219..104330630hg38UCSC Ensembl
Outerchr13:104971569..104982980hg19UCSC Ensembl
Outerchr13:103769570..103780981hg18UCSC Ensembl
Outerchr13:103769570..103780981hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3811412
hg1911412
hg1811412
hg1711412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1163
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)nssv9160
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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