A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9490



Internal ID15539824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:50467455..50515495hg38UCSC Ensembl
Outerchr13:51041591..51089631hg19UCSC Ensembl
Outerchr13:49939592..49987632hg18UCSC Ensembl
Outerchr13:49939592..49987632hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3848041
hg1948041
hg1848041
hg1748041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1040
Supporting Variants
SamplesNA18507
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)nssv9490
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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