A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4707



Internal ID15549443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:9124707..9137477hg38UCSC Ensembl
Outerchr5:9124819..9137589hg19UCSC Ensembl
Outerchr5:9177819..9190589hg18UCSC Ensembl
Outerchr5:9177819..9190589hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3812771
hg1912771
hg1812771
hg1712771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8061
SamplesNA12156
Known GenesSEMA5A
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)nsv4707
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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