A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8096



Internal ID15535768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:39031534..39076232hg38UCSC Ensembl
Outerchr5:39031636..39076334hg19UCSC Ensembl
Outerchr5:39067393..39112091hg18UCSC Ensembl
Outerchr5:39067393..39112091hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3844699
hg1944699
hg1844699
hg1744699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4803
Supporting Variants
SamplesNA12156
Known GenesRICTOR
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)nssv8096
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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