A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139



Internal ID15545702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:97481539..97525876hg38UCSC Ensembl
Outerchr13:98133793..98178130hg19UCSC Ensembl
Outerchr13:96931794..96976131hg18UCSC Ensembl
Outerchr13:96931794..96976131hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3844338
hg1944338
hg1844338
hg1744338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2049
SamplesNA18555
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)nsv1139
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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