A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9120



Internal ID15188058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:48953528..48998591hg38UCSC Ensembl
Outerchr13:49527664..49572727hg19UCSC Ensembl
Outerchr13:48425665..48470728hg18UCSC Ensembl
Outerchr13:48425665..48470728hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3845064
hg1945064
hg1845064
hg1745064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034
Supporting Variants
SamplesNA12156
Known GenesFNDC3A
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)nssv9120
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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