A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153



Internal ID15545716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:101990480..102036171hg38UCSC Ensembl
Outerchr13:102642830..102688521hg19UCSC Ensembl
Outerchr13:101440831..101486522hg18UCSC Ensembl
Outerchr13:101440831..101486522hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3845692
hg1945692
hg1845692
hg1745692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6575
SamplesNA12156
Known GenesFGF14
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)nsv1153
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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